Magic BOOK 3.0 by Dr Nikita
Magic BOOK 3.0 by Dr Nikita
2 Broadmann areas 4
3 Hypothalamus nuclei 5
9 Cadaveric images 10
10 Types of muscle fibers 16
11 Thalamus connections 17
12 Cerebellum 18
B PHYSIOLOGY
13 Darrow yannet diagram 21
14 Baroreceptor 22
15 Renin angiotensin aldosterone system 22
16 Action potential 23
17 Excitation contraction coupling 23
18 O2 hb dissociation curve 24
19 Hypoxia and hypoxemia 25
20 High altitude changes 26
21 Physiology graphs 26
22 Erlanger gasser classification of nerve fibres 29
C BIOCHEMISTRY
23 Summary of pathways 32
24 Krebs cycle 34
25 Urea cycle 34
26 Glycosaminoglycans and MPS 35
27 genetics and molecular biology techniques 37
D FORENSIC MEDICINE
28 Bone age - ossification centres 40
29 Postmortem changes 43
30 Tests for seminal and blood stain 43
31 Autopsy techniques 44
E PHARMACOLOGY
33 Anti arrhythmic drugs 48
34 Hypertension drugs 52
35 Hyperlipidemia types and hypolipidemic drugs 54
36 Anticoagulants 58
37 Hiv drugs 61
38 Asthma treatment 62
39 Anti epileptics 64
40 Antidepressants, Lithium 66
41 Anti psychotics 67
42 Drug schedules 68
43 Diuretics 69
F PSM
44 Post exposure prophylaxis - hiv,rabies, tetanus 73
46 Biostatistics 77
49 Leprosy,nlep, drugs 80
G MICROBIOLOGY
51 Sterilization and disinfectant 86
52 MHC 1 VS MHC 2 88
53 Parvovirus 88
54 AIDs and opportunistic infections 88
55 Plasmodium 90
56 Virology classification, inclusion bodies ,images 90
H PATHOLOGY
57 Interleukins cytokines 95
58 Tumor markers 97
59 Genetic disorders, chromosomes 98
60 Renal casts 101
61 MEN syndrome 103
62 Bleeding disorders 104
I ENT
63 Tympanogram 107
J OPHTHALMOLOGY
65 Astigmatism 110
66 Diabetic retinopathy 110
K PSYCHIATRY
67 Thought disorders 114
L DERMATOLOGY
68 Psoriasis 117
69 Acne vulgaris 117
M ORTHOPEDICS
70 Osteoporosis,including drugs 121
N SURGERY
71 Shock 124
72 Burns 125
73 Breast cancer - everything - staging, classification,treatment 126
P PEDIATRICS
91 Neonatal jaundice 153
92 Newborn resuscitation 154
93 TORCH 154
Q MEDICINE
94 Aphasia 158
95 Pre renal Vs Renal AKI 160
R ANESTHESIA
96 OXYGEN DELIVERY DEVICES 163
97 BLS,ACLS,PALS 164
S RADIOLOGY 168
33. Pellagra 53
34. Amino acid derivatives 54
35. ETC inhibitors 55
36. Inhibitors of glycolysis and TCA 57
37. Enzyme cofactors 58
38. Rate limiting enzymes 59
39. DNA polymerase 60
40. Vitamins 61
41. Vitamin assays 63
42. Glycogen storage disorders 64
43. 66
Lysosomal storage disorders
44. 70
Molecular Biology
D. PATHOLOGY
45. 74
AD/AR/XLR/XLD diseases
46. Trinucleotide repeat disorders 76
47. 77
Anemia
48. 78
CD markers
49. 80
Lymphoma
50. Renal deposits 83
51. 87
Hypersensitivity reactions
E. PHARMACOLOGY
52. Cyp 450 -inducers & inhibitors 90
53. Glaucoma drugs 91
54. 92
DM drugs
55. Vd & clearance 94
56. Graphs - General Pharmacology 95
57. 97
Antifungal drugs
58 Anti TB drugs 99
59. 100
Anticancer drugs
60. Antimicrobials MOA 102
F MICROBIOLOGY
61. Culture media 107
62. 109
Mycology
63. Protozoa 111
64. 113
Rickettsia
65. 114
Hepatitis B serology
Magic Book 2.0- Dr.Nikita Nanwani
66. 116
Parasitology egg tricks
G FMT
67. 119
Plant poison images
68. 120
Aconite poisoning
69. Arsenic & Lead poisoning 121
70. Snake identification 122
71. 123
Drugs of abuse
72. IPC sections 124
H PSM
73. HDI vs PQLI 127
74. Triage 128
75. Biomedical waste management 129
76. Tests of significance 131
77. STI kits 132
78. 133
Vector/ Mosquito
79. Food adulteration diseases 136
I ENT
80. Hearing tests 140
81. Structures opening into Meatus 141
82. X ray views - PNS & orbit 142
J OPHTHALMOLOGY
83 146
Keratoconus
84 Fundus images 148
85. Extra ocular muscles 149
86. Park 3 step test 152
87. Direct vs indirect ophthalmoscopy 153
K MEDICINE
88. ECG - Named waves 156
89. 157
ECG - Supraventricular arrhythmias
90. ECG - Ventricular arrhythmias 158
91. 159
ECG - AV block
92. ECG-MI and PERICARDITIS 160
93. 162
Acid base disorders
94. CURB 65 165
95. Porphyria 166
96. ECG in electrolyte abnormalities 169
97. SAAG 170
Magic Book 2.0- Dr.Nikita Nanwani
98. 171
CSF - meningitis
99. Causes of acidosis / alkalosis 172
100. Renal tubular acidosis (RTA) 173
101. Renal tubular syndromes 174
102. Vasculitis 175
103. 176
Autoimmune diseases with Antibodies
L SURGERY
104. Trauma scoring systems 178
105. GCS 179
106. Liver scoring systems 180
107. Strasberg classification 181
108. Urine crystals 182
109. Upper GI Bleed scores 183
110. 185
IV cannula color coding
111. Vacutainer color coding 186
112. Thyroid scan 187
113. CEAP classification -Chronic venous disease 188
M OBGY
114. Ectopic pregnancy criteria 191
115. Obstetric maneuvers 192
116. Dual/Triple/ Quadruple marker test 194
117. Ovarian tumors classification 195
118 Ovarian tumor - Bodies & tumor markers 196
119. Twins - Lambda vs T sign 198
120. Bishop score 199
121. 200
Vaginal infections
N PEDIATRICS
122. Congenital adrenal hyperplasia 204
123. Malnutrition 205
124. Scores in Pediatrics - APGAR , Silverman Anderson 207
125. Important milestones 208
O DERMATOLOGY
126. STI 212
P PSYCHIATRY
127. Personality disorders 214
Q ORTHOPEDICS
128. 215
Trendelenburg sign
129. Casts , splints, braces 216
130. Named fractures - Upper Limb 219
Magic Book 2.0- Dr.Nikita Nanwani
Stratified squamous
Keratinised strat squamous
Transitional
Pseudostratified columnar ciliated
Simple squamous
URINARY SYSTEM
Table No.1.2
Bowman’s capsule
PCT ,Thick desc limb
Loop of henle
Thick desc limb , DCT
Collecting ducts
Calyx to prostatic urethra
Middle urethra – membranous, Spongy
Terminal urethra
GIT
Table No.1.3
• Tongue
• Esophagus
• Epiglottis
• Anus
• Intestine
RESPIRATORY SYSTEM
Table No.1.4
1
Image No. 1.1
2
Image No. 1.5
Types of glands
Image No. 1.6
3
Types of cartilages
Image No. 1.9
2. Broadmann area
Image No. 1.10 Image No. 2.1
4
3. Hypothalamic nuclei
Image No. 3.1
5
5. Cut section of cerebrum
Image No. 5.1 Image No. 5.2
6
6. Types of white mater
Image No. 6.1
7. Development of diaphragm
Image No. 7
7
7.1Development of IVC
Image No. 7.1
8
8. CRANIAL NERVE COLUMNS AND IDENTIFICATION
Image No. 8.1
9
9. CADAVERIC IMAGES
Image No. 9.1
10
Image No. 9.4
11
Image No. 9.7
12
Image No. 9.10
13
Image No. 9.14
14
Image No. 9.19
15
10. Types of muscle fibres
Image No. 10.1
Table No.10.2
16
11. Thalamus
Images No.11.1
Images No.11.2
17
12. Cerebellum
Images No.12.1 Images No.12.2
Images No.12.3
18
19
20
2. PHYSIOLOGY
13. Darrow Yannet
Table No.13.1
Image No.13.2
Image No.13.3
21
14. Baroreceptor
Image No.14.1
Image No.14.2
22
16. Action Potential
Image No.16.1
Image No17.2
23
18. O2- HB DISSOCIATION CURVE
Image No.18.1
Image No.17.2
Image No.17.3
Image No.17.4
24
19. HYPOXIA AND HYPOXEMIA
Image No.19.1
Image No.19.2
Image No.19.3
25
20. HIGH ALTITUDE CHANGES
Table No.20.1
FIO2 , PIO2
Pao2
ventilation
Paco2
respiratory alkalosis
altitude sickness (headaches, nausea, fatigue, lightheadedness,
sleep disturbance).
erythropoietin
Hct and Hb (due to chronic hypoxia).
2,3-BPG (binds to Hb
shift of oxyhemoglobin dissociation curve
O2 ( release).
Cellular changes ( mitochondria).
renal excretion of HCO3
pulmonary vaso______
_______ ventricular hypertrophy (RVH)
Image No.21.2
Image No.21.3
26
Image No.21.4
Image No.21.5
Image No.21.6
27
Image No.21.7
Image No.21.8
Image No.21.9
Image No.21.10
Image No.21.11
28
Image No.21.12
Image No.21.13
Table No.22.2
Fiber type Function Fiber Conductionvelocity(m/s) Spike
diameter(μm) duration(ms)
Aα Proprioception,somatic 12-20 70-120
motor
Aβ Touch,pressure 5-12 30-70 0.4-0.5
29
30
31
3. BIOCHEMISTRY
23.Summary of pathways
Image No.23.1
32
Image No.23.2
Image No.23.3
Image No.23.4
33
24. Krebs cycle
Image No.24.1
Image No.25.2
34
26. Glycosaminoglycans/Mucopolysaccharidoses
Table No.26.1
Image No.26.2
35
Image No.26.3
Table No.26.1
36
27. MOLECULAR BIOLOGY
37
38
39
4. FORENSIC MEDICINE
28. BONE AGE
Image No. 28.1
Ossification centers of lateral epicondyle, capitulum and trochlea fuse with each
other at about 13–14 years to form a conjoint epiphysis which fuses with shaft at
about 14–15 years
40
Table No. 28.3
Table No.28.5
41
Image No. 28.6
42
29. POST MORTEM LIVIDITY
Table No. 29.1
43
Image No. 30.2
45
46
47
5. PHARMACOLOGY
33. Anti arrhythmic drugs
Table. 33.1
Images 33.2
48
Image 33.3
Image :33.5
49
Table : 33.2
50
Image : 33.6
Image : 33.7
Image : 33.8
Image : 33.9
51
Image : 33.10
Image 33.11
52
Table No: 34.1
Image 34.2
53
35. HYPERLIPIDEMIA CLASSIFICATION AND HYPOLIPIDEMIC DRUGS
Image 35.1
Table No:35.1
54
Drug
Statins
Atorvastatin
Lovastatin, pravastatin,
rosuvastatin
simvastatin
Bile acid resins
Cholestyramine,
Colesevelam,
Colestipol
Ezetimibe
Fibrates
Fenofibrate,
gemfibrozil
Niacin
PCSK9 Inhibitors
Alirocumab,
evolocumab
Fish oil and marine omega-3 fatty acids
Table 35.1
55
56
Table No: 35.2
57
36. Anticoagulants
Image No: 36.1
58
Image No: 36.3
59
Image No: 36.4
60
37. HIV drugs
Image No: 37.1
61
38. Asthma drugs
Image No: 38.1
62
Image No: 38.2
63
39. Anti epileptics
Image No: 39.1
64
Image No: 39.3
65
40. Anti depressants
Image No: 40.1
66
41. Antipsychotics
Image No: 41.1
67
42. Drug schedules
68
43. Diuretics
Image No: 43.1
69
Table No: 43.1
DRUG OF CHOICE
70
71
72
6. PSM
44. POST EXPOSURE PROPHYLAXIS - HIV,RABIES, TETANUS HIV
Table No: 44.1
TETANUS
Table No: 44.2
RABIES
73
Table No: 44.2
TYPE OF ROUTE OF DOSE OF DAY OF NO OF TOTA SITE OF
PROPHYLA ADMINISTRATI VACCINE DOSE INJECTI L NO INJECTION
XIS ON ON PER
VISIT
POST INTRA 0.1ML 0,3,7,28 2 4 ADULTS:
EXPOSURE DERMAL DOSE DELTOID
PROPHYLA MUSCLE
XIS O,3,7,14,28 1 5
INTRA 1ENTIRE INFANTS
MUSCULAR VACCINE &CHILDREN:
VIAL ANTEROLATE
RAL THIGH
PRE INTRA 0.1ML 0,7&BOOST 1 3
EXPOSURE DERMAL DOSE ER DOSE
PROPHYLA ON 21 OR
XIS 1 ENTIRE 28 1 3
INTRA VACCINE 0,7&BOOST
MUSCULAR VIAL ER ON 21
OR 28
RE INTRADERMA 0.1MLDO DAY 0&3 1 2
EXPOSURE L SE
1 ENTIRE
INTRAMUSCU VACCINE DAY0&3 1 2
LAR VIAL
74
45. NATIONAL IMMUNISATION SCHEDULE
Table :45.1
75
76
46. BIOSTATISTICS
Image No: 46.1
Image No:46.3
77
Image No: 46.4
47. Screening
Image No: 47.1
78
Image No: 47.2
79
49. LEPROSY
Who approved treatment for multibacillary leprosy
Age group Drug Duration of treatment
Adult Rifampicin 600 mg once a month + 12
Clofazimine 300 mg once a month months(Multibacillary)
and 50 mg daily 6
+ months(Paucibacillary)
Dapsone 100 mg daily
Children (10-14 years) Rifampicin 450 mg once a month + 12
Clofazimine 150 mg once a month months(Multibacillary)
and 50 mg alternate days. + 6
Dapsone 50 mg daily months(Paucibacillary)
Children <10 years old or Clofazimine 100mg once a month, 12
<40kg 50mg twice weekly months(Multibacillary)
+ 6 months(Paucibacillary
Dapsone 2 mg/kg daily
80
Image No: 49.1
81
82
50. NTEP
83
84
85
7.MICROBIOLOGY
86
QUALITY CONTROL AGENTS
Hot oven: Bacillus atropheus subspecies niger
Autoclave : Geobacillus stearothermophilus
Radiation: Bacillus pumilus
Filtration: Serratia marcescans Brevundimonas dimunita
Ethylene oxide (Eto) : B. atropheus subspecies globigii
87
52. MHC VS MHC 2
53. PARVOVIRUS
88
PNEUMOCYSTIS JIROVECI
89
55. PLASMODIUM
90
INCLUSION BODIES
Negri bodies
91
MOLLUSCUM CONTAGIOSUM
92
93
94
8. PATHOLOGY
57. Interleukin and cytokines
95
96
58. Tumor markers
Alkaline phosphatase
α-fetoprotein
hCG
CA15-3/CA27-29
CA 19-9
CA 125
Calcitonin
CEA
Chromogranin
LDH
Neuron-specific enolase
PSA
Immunohistochemical stains
Chromogranin and synaptophysin
Cytokeratin
Desmin
GFAP
Neurofilament
PSA
PECAM-1/CD-31
S-100
TRAP
Vimentin
97
59. GENETIC DISORDERS
98
GENETIC DISORDERS BY CHROMOSOME
MODES OF INHERITANCE
Autosomal dominant
Autosomal recessive
99
X linked recessive
Mitochondrial inheritance
100
60. Renal casts
RBC casts
WBC casts
Granular casts
Hyaline casts
101
102
61MEN SYNDROMES
MEN1 Pituitary tumors (prolactin or GH)
Pancreatic endocrine tumors—Zollinger-Ellison syndrome, insulinomas, VIPomas, glucagonomas
(rare)
Parathyroid adenomas
Associated with mutation of MEN1 (tumor suppressor, codes for menin, chromosome 11),
angiofibromas, collagenomas, meningiomas
MEN2A Parathyroid hyperplasia
Medullary thyroid carcinoma—neoplasm of parafollicular C cells; secretes calcitonin; prophylactic
thyroidectomy required
Pheochromocytoma (secretes catecholamines)
Associated with mutation in RET (protooncogene, codes for receptor tyrosine kinase, chromosome
10)
Medullary thyroid carcinoma
Pheochromocytoma
Mucosal neuromas (oral/intestinal ganglioneuromatosis)
Associated with marfanoid habitus; mutation in RET gene.
MEN2B
103
62. Bleeding disorders
104
105
106
9. ENT
63. TYMPANOGRAM
64. CALARYNX
107
108
109
10.OPHTHALMOLOGY
65. ASTIGMATISM
66.Diabetic retinopathy
110
111
112
113
11.PSYCHIATRY
67.Disorders of thought
114
115
116
12.DERMATOLOGY
68. PSORIASIS
117
69.Acne vulgaris
118
119
120
13.ORTHOPEDICS
70.OSTEOPOROSIS
121
122
123
14. SURGERY
71. SHOCK
124
72. BURNS
125
73.BREAST CANCER
126
127
74. NAMED SURGERIES
Hadfeild Sx
Orringer Sx
Longo Procedure
Patey's Sx
Sistrunk’s Sx
Frey procedure
Whipples Sx
Ladd's Procedure
Milligan Morgan operation
Kasai procedure.
Bishop Koop operation
Duhamel, Swensen and Soave Operations
Strong Procedure
Palomo Operation
Palma Operation
Nesbitt Operation
Gray hack Shunt operation
Dennis Brown Operation
Anderson Hynes Operation
Hellers Cardiomyotomy
POEM
Stretta Procedure
Nissen Fundoplication
Belsey Mark 4 Operation
Ivor Lewis Operation
128
75. NAMED HERNIA
129
130
131
77. ATLS(TRAUMA)
132
133
134
135
136
15.OBG
CANCER STAGING
78.CACERVIX
79. Ca endometrium
Ca ovary
137
Ca vulva
138
PAP smear , HPV vaccine
139
82.Molar pregnancy
140
83. Placenta abnormalities
84.Contraception
141
142
85. Primary amenorrhea
Diagnosis:
Biochemical hyperandrogenemia ↑ testosterone (total +/− free),
DHEAS.
Other causes of hyperandrogenism TSH, prolactin.
17-OH progesterone to rule out nonclassical CAH.
Consider screening in the setting of clinical signs of
Cushing’s syn- drome (eg, moon facies, buffalo hump,
abdominal striae) or acromeg- aly (eg, ↑ head size).
Metabolic abnormalities Two-hour oral glucose tolerance test.
Fasting lipid and lipoprotein levels (total cholesterol, HDL,
LDL, tri-glycerides).
Optional tests Ultrasound: Look for > 8 small, subcapsular follicles
forming a "pearl necklace" sign.
Seen in roughly two-thirds of
women with PCOS.
Gonadotropins: ↑ LH/FSH ratio (>2:1).
24-hour urine for free cortisol: Adult-onset CAH or
Cushing's syndrome.
143
Treatment:
Women who are not attempting to conceive Treat with a combination of OCPs, progestin, and
metformin (or other insulin-sensitizing agents).
Women who are attempting to conceive Clomiphene +/- metformin is first-line treatment
for ovulatory stimulation
Symptom-specific treatment HIRSUTISM: Combination OCPs are first line;
antiandrogens (spirono- lactone, finasteride) and
metformin may also be used.
CARDIOVASCULAR RISK FACTORS AND LIPID
LEVELS: Diet, weight loss, and exercise plus
potentially lipid-controlling medication (eg,
statins).
144
87. GESTATIONAL DIABETIS MELLITUS
Diabetes in pregnancy
Gestational Pregestational
Conduct a 1-hour 50-g glucose challenge 1. Venous plasma glucose is measured I hour
test later.
2. Performed at 24-28 weeks.
3. Values ≥ 140 mg/dl are considered
abnormal.
145
88. RH NEGATIVE MOTHER
Definition
Diagnosis:
Treatment:
Prevention:
Complications:
146
89. PRE ECLAMPSIA, MGSO4
preeclampsia
Severe preeclampsia
eclampsia
Mgso4
147
90. PHYSIOLOGICAL CHANGES IN PREGNANCY
148
CHANGES IN BREAST
UTERINE CHANGES:
INCREASED DECREASED
149
RESPIRATORY CHANGES IN PREGNANCY
INCREASED DECREASED
150
151
152
16. PAEDIATRICS
153
92. Neonatal resuscitation
93. TORCH
TORCH INFECTIONS
CONGENITAL TOXOPLASMOSIS
CLINICAL TRIAD- CHORIORETINITIS , HYDROCEPHALUS, CEREBRAL CALCIFICATIONS
TOXOPLASMOSIS – MACROCEPHALY (Hydrocephalus)
HEADLIGHT IN FOG APPEARENCE
CONGENITAL RUBELLA
C- CATARACT
154
CMV
90% are Asymptomatic
Developing countries – reactivation of CMV infection of mother
PeriVentricular calcifications,microcephaly ,chorioretinitis
S – SNHL(non syndromic)
Most children symptomatic at birth develops hearing loss
Incidence of CMV infection in fetus with mainly primary infection
Herpes zoster
Limb hypoplasia
Zika virus
Aydes aegyptie mosquito
Hoffbauer cell in placental tissue
Feature –
Microcephaly (HC <-3SD) AND Micrencephaly
Macular scarring
Hypertonia and limb deformities (CTEV)
Subcortical calcifications
Congenital Syphilis
Late (>2yrs)
Hutchison triad
Teeth (notching / peg shaped incisors )
Interstitial keratitis
Deafness
Mulberry molars
Fissure – Rhagades
155
156
157
17. MEDICINE
94. APHASIA
158
159
95. Pre renal vs renal AKI
160
161
162
18. ANAESTHESIA
96. OXYGEN DELIVERY DEVICES
163
97. BLS ACLS
164
165
166
167
19. RADIOLOGY
168
169
170
171
172
173
174
175
176
177
178
179
180
Boston brace
Taylor brace
Milwaukee Brace
Galeazzi Fracture
181
Reticulin stain
182
Ebola Virus Disease
Schistosoma haematobium
Dermatitis herpetiforms
Trichuris trichiura
183
Reticulin Stain
Hess chart
184
Synoptophore
Dermatitis Herpetiformis
Lichen nitidus
Book test
185
Ecg psvt
Neisseria gonorhhea
Ecg VT
186
Pseudomonas Oxidase Positive
Chromoblastomycosis
187
Ecg hyperkelemia
Genital herpes
Kf ring
188
Shawl sign dermatomyositis
Lilac rash
Sporotrichosis
189
Dermatomyositis
Orange foleys
Green cannula
190
Maddox rod
Fincham test
Pawlik grip
191
Stargardts disease
Goldman tonometer
193
sporotrichosis
Romovac suction
194
CLINICAL PRESENTATION
DIAGNOSIS /DISEASE CLINICAL PRESENTATION
Anaphylaxis following blood transfusion IgA deficiency
Aortic regurgitation Bounding pulses, wide pulse pressure, diastolic heart
murmur, head bobbing
Aortic stenosis Systolic ejection murmur (crescendo-decrescendo),
narrow pulse pressure, pulsus parvus et tardus
Angina (stable: with moderate exertion; unstable: Chest pain on exertion
with minimal exertion or at rest)
Angina (⊝ troponins) or NSTEMI (⊕ troponins) Chest pain with ST depressions on ECG
Acute adrenal insufficiency Shock, altered mental status, vomiting, abdominal
pain, weakness, fatigue in patient under
glucocorticoid therapy
Anterior drawer sign ⊕ Anterior drawer sign ⊕
Alport syndrome (mutation in type IV collagen) Hereditary nephritis, sensorineural hearing loss,
retinopathy, anterior lenticonus
Alkaptonuria (homogentisate oxidase deficiency; Bluish-black connective tissue, ear cartilage, sclerae;
ochronosis) urine turns black on prolonged exposure to air
Becker muscular dystrophy (X-linked non-frameshift Slow, progressive muscle weakness in boys
deletions in dystrophin; less severe than Duchenne)
Babinski sign (UMN lesion) Dorsiflexion of large toe with fanning of other toes
upon plantar scrape
Bowlegs (children), bone pain, and muscle weakness Rickets (children), osteomalacia (adults); vitamin D
deficiency
Recurrent Neisseria infection Terminal complement deficiencies (C5-C9)
Beck triad of cardiac tamponade Distant heart sounds, distended neck veins,
hypotension
Burton line (lead poisoning) Bluish line on gingiva
B symptoms of malignancy Fever, night sweats, weight loss
Basal ganglia lesion Resting tremor, athetosis, chorea
Beckwith-Wiedemann syndrome (WT2 mutation) Wilms tumor, macroglossia, organomegaly,
hemihyperplasia, omphalocele
Mucor or Rhizopus fungal infection Black eschar on face of patient with diabetic
ketoacidosis and/or neutropenia
Cri-du-chat (cry of the cat) syndrome Microcephaly, high-pitched cry, intellectual disability
Cori disease (debranching enzyme deficiency) or Infant with hypoglycemia, hepatomegaly
Von Gierke disease (glucose-6-phosphatase
deficiency, more
severe)
Chronic granulomatous disease (defect of NADPH Recurrent infections and granulomas with catalase ⊕
oxidase) organisms
Clostridioides difficile infection Abdominal pain, diarrhea, leukocytosis, recent
antibiotic
Use
Corynebacterium diphtheria infection Tonsillar pseudomembrane with “bull’s neck”
appearance
Condylomata lata (2° syphilis) Smooth, moist, painless, wartlike white lesions on
genitals
Coxsackie A, 2° syphilis, Rocky Mountain spotted Rash on palms and soles
fever
Cystic fibrosis (CFTR gene defect, chromosome 7, Meconium ileus in neonate, recurrent pulmonary
ΔF508) infections, nasal polyps, pancreatic insufficiency,
infertility/subfertility
Chorioretinitis, hydrocephalus, intracranial Congenital toxoplasmosis
calcifications
Chvostek sign (hypocalcemia) Facial muscle spasm upon tapping
Carcinoid syndrome ( urinary 5-HIAA) Cutaneous flushing, diarrhea, bronchospasm, heart
murmur
DIAGNOSIS /DISEASE CLINICAL PRESENTATION
Chronic 1° adrenal insufficiency (Addison disease) Skin hyperpigmentation, orthostatic hypotension,
ACTH, MSH fatigue,
weakness, muscle aches, weight loss, GI
disturbances
Courvoisier sign (distal malignant obstruction of Jaundice, palpable distended non-tender gallbladder
biliary
tree)
Crigler-Najjar syndrome (congenital unconjugated Severe jaundice in neonate
hyperbilirubinemia)
Cholelithiasis (gallstones) Female, fat (obese), fertile (multiparity), forty, fair
Cancer of the pancreatic head obstructing bile duct Painless jaundice with enlarged gallbladder
Cold agglutinin disease (autoimmune hemolytic Paroxysmal nocturnal hemoglobinuria
anemia caused by Mycoplasma pneumoniae,
infectious mononucleosis, CLL)
Cerebellar lesion (lateral affects voluntary movement Truncal ataxia, nystagmus, head tilting, fall towards
of extremities; medial affects axial and proximal injured side
movement)
Chronic bronchitis (hypertrophy and hyperplasia of Hypoxemia, polycythemia, hypercapnia
mucus-secreting glands, “blue bloater”)
Duchenne muscular dystrophy (Gowers sign) Child uses arms to stand up from squat
Down syndrome Single palmar crease, intellectual disability
Dressler syndrome (autoimmune-mediated post-MI Chest pain, pericardial effusion/friction rub, persistent
fibrinous pericarditis, 2 weeks to several months after fever following MI
acute episode)
Diabetic ketoacidosis (Kussmaul respirations) Rapid, deep, labored breathing/hyperventilation
Delirium (usually 2° to other cause) “Waxing and waning” level of consciousness (acute
onset), attention span, level of arousal
Ehlers-Danlos syndrome (type V collagen defect, Elastic skin, hypermobility of joints, bleeding
type III tendency
collagen defect seen in vascular subtype of ED)
Edwards syndrome (trisomy 18) Infant with microcephaly, rocker-bottom feet,
clenched
hands, and structural heart defect
Erb-Duchenne palsy (superior trunk [C5–C6] brachial Neonate with arm paralysis following difficult birth,
plexus injury) arm
in “waiter’s tip” position
Epidural hematoma (middle meningeal artery Lucid interval after traumatic brain injury
rupture; branch of maxillary artery)
Emphysema (“pink puffer,” centriacinar [smoking] or Pink complexion, dyspnea, hyperventilation
panacinar [α1-antitrypsin deficiency])
Familial hypercholesterolemia ( LDL receptor Achilles tendon xanthoma
signaling)
Fanconi anemia (genetic loss of DNA crosslink Short stature, cafe-au-lait spots, thumb/radial
repair; often progresses to AML) defects, incidence of tumors/leukemia, aplastic
anemia
Fanconi syndrome (multiple combined dysfunction of Polyuria, renal tubular acidosis type II, growth
the proximal convoluted tubule) retardation,
electrolyte imbalances, hypophosphatemic rickets
Clostridium botulinum infection (floppy baby Flaccid paralysis in newborn after ingestion of honey
syndrome)
Jarisch-Herxheimer reaction (due to host response to Fever, chills, headache, myalgia following antibiotic
sudden release of bacterial antigens) treatment for syphilis
Friedreich ataxia Staggering gait, frequent falls, nystagmus, hammer
toes, diabetes mellitus, hypertrophic cardiomyopathy
Gaucher disease (glucocerebrosidase [β- Hepatosplenomegaly, pancytopenia, osteoporosis,
glucosidase] deficiency) avascular necrosis of femoral head, bone crises
Guillain-Barre syndrome (acute inflammatory Rapidly progressive limb weakness that ascends
demyelinating polyneuropathy) following GI/upper respiratory infection
Gout/podagra (hyperuricemia) Sudden swollen/painful big toe joint, tophi
DIAGNOSIS /DISEASE CLINICAL PRESENTATION
Gardner syndrome (subtype of FAP) Multiple colon polyps, osteomas/soft tissue tumors,
impacted/supernumerary teeth
Homocystinuria (autosomal recessive) Arachnodactyly, pectus deformity, lens dislocation
(downward)
Hookworm (Ancylostoma spp, Necator americanus) Pruritus, serpiginous rash after walking barefoot
Child with fever later develops red rash on face that Erythema infectiosum/fifth disease (“slapped cheeks”
spreads to body appearance, caused by parvovirus B19)
Hyperthyroidism Heat intolerance, weight loss, palpitations
Hypothyroidism Cold intolerance, weight gain, brittle hair
Huntington disease (autosomal dominant CAG Chorea, dementia, caudate degeneration
repeat expansion)
Horner syndrome (sympathetic chain lesion) Ptosis, miosis, anhidrosis
Hereditary hemorrhagic telangiectasia (Osler-Weber- Telangiectasias, recurrent epistaxis, skin
Rendu syndrome) discoloration,
arteriovenous malformations, GI bleeding, hematuria
Immunoglobulin A vasculitis (Henoch-Schonlein Palpable purpura on buttocks/legs, joint pain,
purpura, affects skin and kidneys) abdominal pain (child), hematuria
Infective endocarditis Splinter hemorrhages in fingernails
Internuclear ophthalmoplegia (damage to MLF; may Conjugate horizontal gaze palsy, horizontal diplopia
be unilateral or bilateral)
Janeway lesions (infective endocarditis, septic Painless erythematous lesions on palms and soles
emboli/ microabscesses)
Klebsiella pneumoniae pneumonia Waterhouse-Friderichsen syndrome
(meningococcemia)
Red “currant jelly” sputum in patients with alcohol Klebsiella pneumoniae pneumonia
overuse or diabetes
Kawasaki disease (mucocutaneous lymph node Cervical lymphadenopathy, desquamating rash,
syndrome, treat with IVIG and aspirin) coronary aneurysms, red conjunctivae and tongue,
hand-foot changes
Kaposi sarcoma, associated with HHV-8 Dark purple skin/mouth nodules in a patient with
AIDS
Kluver-Bucy syndrome (bilateral amygdala lesion) Babinski sign (UMN lesion)
Koplik spots (measles [rubeola] virus) Small, irregular red spots on buccal/lingual mucosa
with
blue-white centers
Lesch-Nyhan syndrome (HGPRT deficiency, X-linked Gout, intellectual disability, self-mutilating behavior in
recessive) a boy
Erythema migrans from Ixodes tick bite (Lyme Large rash with bull’s-eye appearance
disease: Borrelia)
Lower GI bleeding (eg, colonic diverticulosis) Hematochezia
Lichen planus Kaposi sarcoma, associated with HHV-8
Lateral medullary (Wallenberg) syndrome (posterior Dysphagia, hoarseness, gag reflex, nystagmus,
inferior cerebellar artery lesion) ipsilateral Horner syndrome
LMN damage Hyporeflexia, hypotonia, atrophy, fasciculations
LMN facial nerve (CN VII) palsy; UMN lesions spare Unilateral facial drooping involving forehead
the Forehead
Leukocyte adhesion deficiency (type 1; defective Late separation (>30 days) of umbilical cord, no pus,
LFA-1 integrin) recurrent skin and mucosal bacterial infections
Marfan syndrome (fibrillin defect) Arachnodactyly, lens dislocation (upward and
temporal), aortic dissection, hyperflexible joints
McCune-Albright syndrome (Gs-protein Cafe-au-lait spots (unilateral), polyostotic fibrous
dysplasia, precocious puberty, multiple endocrine
abnormalities
Muscular dystrophy (most commonly Duchenne, due Calf pseudohypertrophy
to X-linked recessive frameshift mutation of
dystrophin gene)
McArdle disease (skeletal muscle glycogen Chronic exercise intolerance with myalgia, fatigue,
phosphorylase painful cramps, myoglobinuria
deficiency)
DIAGNOSIS /DISEASE CLINICAL PRESENTATION
Mycoplasma pneumoniae infection Atypical "walking pneumonia" with x-ray looking
worse than the patient
Myxedema (caused by hypothyroidism, Graves Cutaneous/dermal edema due to deposition of
disease [pretibial]) mucopolysaccharides in connective tissue
MEN1 (autosomal dominant MEN1 mutation) Pancreatic, pituitary, parathyroid tumors
MEN2A (autosomal dominant RET mutation) Thyroid and parathyroid tumors, pheochromocytoma
MEN2B (autosomal dominant RET mutation) Thyroid tumors, pheochromocytoma,
ganglioneuromatosis, Marfanoid habitus
Mallory-Weiss syndrome (alcohol use disorder, Vomiting blood following gastroesophageal
bulimia nervosa) lacerations
Male child, recurrent infections, no mature B cells Bruton disease (X-linked agammaglobulinemia)
McBurney sign (acute appendicitis) Severe RLQ pain with deep tenderness
Mycosis fungoides (cutaneous T-cell lymphoma) or Skin patches/plaques, Pautrier microabscesses,
Sezary syndrome (mycosis fungoides + malignant atypical T cells
T cells in blood)
Multiple sclerosis Nystagmus, intention tremor, scanning speech,
bilateral internuclear ophthalmoplegia
Meniere disease Episodic vertigo, tinnitus, sensorineural hearing loss
Meigs syndrome Ovarian fibroma, ascites, pleural effusion
Measles Fever, cough, conjunctivitis, coryza, diffuse rash
Nonpainful, indurated: chancre (1° syphilis, Ulcerated genital lesion
Treponema pallidum) Painful, with exudate:
chancroid (Haemophilus ducreyi)
Neurosyphilis (Argyll Robertson pupil) Pupil accommodates but doesn’t react to light
Normal pressure hydrocephalus Urinary incontinence, gait apraxia, cognitive
dysfunction
Neurofibromatosis type I Cafe-au-lait spots, Lisch nodules (iris hamartoma),
cutaneous neurofibromas, pheochromocytomas,
optic gliomas
Nevus flammeus (benign, but associated with Sturge- Vascular birthmark (port-wine stain) of the face
Weber syndrome)
Nephrotic syndrome Periorbital and/or peripheral edema, proteinuria (>
3.5g/ day), hypoalbuminemia, hypercholesterolemia
Osteogenesis imperfecta (type I collagen defect) Blue sclera, multiple fractures, dental problems,
conductive hearing loss
Osler nodes (infective endocarditis, immune complex Painful, raised red lesions on pads of fingers/toes
deposition)
Osteitis deformans (Paget disease of bone, Bone pain, bone enlargement, arthritis
osteoblastic and osteoclastic activity)
Osteoarthritis (osteophytes on PIP [Bouchard nodes], Swollen, hard, painful finger joints in an elderly
DIP [Heberden nodes]) individual, pain worse with activity
Patau syndrome (trisomy 13) Infant with cleft lip/palate, microcephaly or
holoprosencephaly, polydactyly, cutis aplasia
Phenylketonuria Intellectual disability, musty body odor,
hypopigmented skin, eczema
Pompe disease (lysosomal α-1,4-glucosidase Myopathy (infantile hypertrophic cardiomyopathy),
deficiency) exercise intolerance
Pott disease (vertebral TB) Back pain, fever, night sweats
Pasteurella multocida (cellulitis at inoculation site) Dog or cat bite resulting in infection (cellulitis,
osteomyelitis)
PDA (close with indomethacin; keep open with PGE Continuous “machinelike” heart murmur
analogs)
Primary polydipsia, diabetes insipidus (central, Polyuria (water diuresis), polydipsia
nephrogenic)
Plummer-Vinson syndrome (may progress to Dysphagia (esophageal webs), glossitis, iron
esophageal squamous cell carcinoma) deficiency anemia
Peutz-Jeghers syndrome (inherited, benign polyposis Hamartomatous GI polyps, hyperpigmented macules
can cause bowel obstruction; breast/GI cancer risk) on mouth, feet, hands, genitalia
Paroxysmal nocturnal hemoglobinuria Red/pink urine, fragile RBCs
DIAGNOSIS /DISEASE CLINICAL PRESENTATION
Platelet disorders (eg, Glanzmann thrombasthenia, Petechiae, mucosal bleeding, prolonged bleeding
Bernard Soulier, HUS, TTP, ITP, uremic platelet time
dysfunction)
Paget disease of the breast (sign of underlying Red, itchy, swollen rash of nipple/areola
neoplasm)
Parkinson disease (loss of dopaminergic neurons in Resting tremor, rigidity, akinesia, postural instability,
substantia nigra pars compacta) shuffling gait, micrographia
Peyronie disease (connective tissue disorder) Fibrous plaques in tunica albuginea of penis with
abnormal curvature
Pellagra (niacin [vitamin B3] deficiency) Dermatitis, dementia, diarrhea
Roth spots (infective endocarditis) Retinal hemorrhages with pale centers
Rovsing sign (acute appendicitis) Severe RLQ pain with palpation of LLQ
Raynaud phenomenon (vasospasm in extremities) Painful fingers/toes changing color from white to blue
to red with cold or stress
Recurrent cold (noninflamed)abscesses, eczema, Hyper-IgE syndrome (Job syndrome: neutrophil
high serum IgE, eosinophils chemotaxis abnormality)
Situs inversus, chronic ear infections, sinusitis, Primary ciliary dyskinesia or Kartagener syndrome
bronchiectasis, infertility (dynein arm defect affecting cilia)
Scurvy (vitamin C deficiency: can’t hydroxylate Swollen gums, mucosal bleeding, poor wound
proline/ healing,
lysine for collagen synthesis); tea and toast diet petechiae, corkscrew hairs
Staphylococcal toxic shock syndrome Fever, vomiting, diarrhea, desquamating rash
following use of nasal pack or tampon
Scarlet fever (sandpaper rash); Kawasaki disease “Strawberry tongue”
(lymphadenopathy, high fever for 5 days)
Streptococcus bovis Colon cancer associated with infective endocarditis
Sheehan syndrome (severe postpartum hemorrhage No lactation postpartum, absent menstruation, cold
leading to pituitary infarction) Intolerance
Sjogren syndrome (autoimmune destruction of Dry eyes, dry mouth, arthritis
exocrine glands)
Reactive arthritis associated with HLA-B27 Urethritis, conjunctivitis, arthritis in a male
Systemic lupus erythematosus “Butterfly” facial rash, arthritis, cytopenia, and fever in
a young female
Sarcoidosis (noncaseating granulomas) Bilateral hilar adenopathy, uveitis
Tay-Sachs (ganglioside accumulation; no “Cherry-red spots” on macula
hepatosplenomegaly); Niemann-Pick disease
(sphingomyelin accumulation; hepatosplenomegaly);
central retinal artery occlusion
Terminal complement deficiencies (C5-C9) Recurrent Neisseria infection
Turner syndrome (45,XO) Streak ovaries, congenital heart disease, horseshoe
kidney, cystic hygroma, short stature, webbed neck,
lymphedema
Trousseau sign (hypocalcemia) Carpal spasm upon inflation of BP cuff
Upper GI bleeding (eg, peptic ulcer disease) Hematemesis, melena
UMN damage Hyperreflexia, hypertonia, Babinski sign present
Vitamin B5 deficiency Burning feet syndrome
Vitamin K deficiency Hemorrhagic disease of newborn with PT, a PTT
Virchow node (abdominal metastasis) Enlarged, hard left supraclavicular node
von Hippel-Lindau disease (deletion of VHL on Renal cell carcinoma (bilateral),
chromosome 3p) hemangioblastomas,
angiomatosis, pheochromocytoma
Bilateral vestibular schwannomas Neurofibromatosis type II
Wernicke encephalopathy (add Confusion, ophthalmoplegia/nystagmus, ataxia
confabulation/memoryloss for Korsakoff syndrome)
Wet beriberi (thiamine [vitamin B1] deficiency) Dilated cardiomyopathy/high-output heart failure,
edema, alcoholism or malnutrition
DIAGNOSIS /DISEASE CLINICAL PRESENTATION
Waterhouse-Friderichsen syndrome Adrenal insufficiency, fever, DIC
(meningococcemia)
Whipple disease (Tropheryma whipplei) Arthralgias, adenopathy, cardiac and neurological
symptoms, diarrhea
Wilson disease (Kayser-Fleischer rings due to copper Golden brown rings around peripheral cornea
accumulation)
“Worst headache of my life” Subarachnoid hemorrhage
CLASSIC LABS / FINDINGS
DIAGNOSIS /DISEASE LAB /DIAGNOSTIC
FINDING
“Apple core” lesion on Colorectal cancer (usually
barium enema x-ray left-sided)
ADHD Methylphenidate,
amphetamines, behavioral
therapy,
atomoxetine, guanfacine,
clonidine
Alcohol use disorder Disulfiram, acamprosate,
naltrexone, supportive care
Hyperaldosteronism Spironolactone
Hypercholesterolemia Statin (first-line)
Hypertriglyceridemia Fibrate
Hypochromic, microcytic Iron deficiency anemia, lead
anemia poisoning, thalassemia (fetal
hemoglobin sometimes
present)
2 Types of cartilage
3 Muscles of larynx
4 Cerebrum cut section spotter, coronal section of brain spotter
5 Muscles of mastication spotter
6 Reticular fibres of collagen
7 Foramen in skull spotter ,structure passing through skull
foramina
8 Types of joints ,classification of synovial joints, fibrous joints
9 Corpus callosum spotter
10 Types of glands
11 Cvs embryology foramen and lesser sac
12 Relations of epiploic foramen and lesser sac
13 H/P section of cerebellum and it’s nuclei
14 Cerebellar circuit ,layers ,cells of cerebellum
15 Muscles of abdomen, conjoint tendon spotter
16 Pharyngeal pouch derivatives
17 Nerve injuries also written in ortho
18 Pelvic diaphragm
19 Cerebrum and broadman’s area ,aphasia
20 Supracondylar humerus # and nerve injuries also written in
ortho
21 Cranial nerves/ origin spotters/ cut section of brain/foramina
related to it
22 Azygos system of veins
23 Muscles of gluteal region
24 Palmar nd dorsal interossei
25 Brachial Plexus
26 Relations of Kidney,stomach, liver all organs of abdomen
27 Pterion spotter
28 Deep cervical fascia
29 Carotid sheath and triangle of neck
30 Muscle attachment of femur
31 Blood supply of tonsils
32 Internal iliac artery branches
33 Spermatogenesis
34 NCC derivatives
5
Paul bunnell test
6 Sterilisation and disinfectant
7 M.Tb
8 Aspergillosis
9 Chromblastomycosis
10 Pneumocystis jiroveci
11 Histoplasma capsultum
12 Nocardia
13
Zika fever and virus
14 H.nana
15 E.coli
16 Influenza virus
17
Syphillis nd darkfield microscopy
18 N.gonorrhoea
19 Echinococcus
20 Xenodiagnostic method
21 SARS cov 2
23
Scrub typhus
Pathology-
1 Membranous nephropathy
2 Urinary cast – maltese cross
General pathology
1 T helper cells types and differences
2 Apoptosis
3 Types of calcification
4 Flowcytometry – hyper lgM syndrome
5 Immunodeficiency disorder
6 Anaphylactoid reaction
7 Cytokins and interleukin
8 Hypersensitivity types
9 Tumor suppressor genes and growth factor receptor and
associated tumours and oncogene – associated cancer tables
10 Graft vs host disease
11 Wiskott aldrich syndrome
Hematology
Pathology-
1 Staining and fixation –sweet reticulum stain, acetone free
methanol used in fixation,staining techniques and cell/inclusion
stained complete list
2 Iron deficiency anemia
3 AML/ALL/CML/SLL/CLL
4 Polycythemia
5 Multiple meloma
6 NLPHL
7 NHL/HL
8 Storage of blood- CDPA
9 Extrinsic and intrinsic Pathway
10 Mantle cell lymphoma and other lymphoma too
11 Blood component – storage temperature
12 Vaccutainers and use
13 Iron absorption
14 TACO
15 Blood transfusion reaction
16 Bone marrow biopsy needle
17 G6pd deficiency
18 Thromboelastography
19 LCH- birbeck granules and whole topic
20 Blood transfusion screening
21 Corrected reticulocyte count
Rheumatology /Bone
Pathology
1 SLE
Endocrine
Pathology
1 Cancer of thyroid proto-oncogene
2 Acromegaly
Respiratory
Pathology-
1 Asbestosis
2 Covid 19
3 Cystic fibrosis
4 SCC lung
4
ATLS
5
During inguinal hernia operation nerve involved
6 Acute appendicitis and it’s signs
7 Southampton grading
8
Chest tube
9 Obstructive jaundice
10 Thyroid Cancer
11 I/V cannula also written in Anesthesia
12 Foleys catheter
13 Triage
14 Psoas abscess
15 Bile duct injury management
16 Triangle of Doom
17 Tension pneumothorax
18 Ryle’s tube
19 Thyroid storm
20 GCS
21 Achalasia cardia
22 Thymoma
23 qSOFA
24
SIRS
25 Variceal bleeding management
26
Pneumoperitoneum- veress neddle spotter
27 Nerve injured in thyroid sx
28 Colon ca
29
Bile duct injury classification
30 CEAP
31 CHPS
32 Pneumoperitoneum management
33 Hollow viscus perforation X-ray
34 PUV
35
RTA management
36
Appendectomy
Medicine
1 Hypothyroidism
2 Grave’s disease
3 DM drugs,screening of DM
4 Vitamin D toxicity
5 MEN syndrome
Medicine
1 DIC
2 Haemophilia
Infections
Medicine-
1 Doc for scrub typhus
2 Infection post organ transplant
3 ATT and ART
4 AIDS defining malignancy
5 HIV and prophylaxis for various organisms
Neurology
1 GBS –myelinated axon electron microscope appearance spotter
Medicine-
1 Parkinson –Paralysis
2 Thrombolysis stroke and management
3 Ischemic stroke and management
4 CSF finding in meningitis
5 Central pontine myelinolysis
6 Anti epileptic drugs
7 Spinal card tracts and localization of lesions
8 Neuromyelitis optica
9 Lateral medullary syndrome
10 Types of headache
11 Seizure
12 Clinical examination for umn lesion ,babinski sign spotter
13 Internal capsule, types of lacunar syndrome
Medicine-
1 ATT ,role of pyridoxine
2 Flow volume curve
3 CAP
4 Pleural effusion
5 PFT of obstructive and restrictive
6 FEV1/FVC
Core medicine topics
1 Electrolytes imbalance- hypo/hyperkalemia ,
hyper/hypocalcemia, hyponatremia
2 ABG
3 Anion gap
Nephrology
Medicine-
1 AKL and it’s criteria
Liver/git
1 Esophageal Cancer –SCC, AdenoCa
2 Barrett esophagus
3 Celiac disease
4 Peutz- jeghers syndrome
Medicine-
1 Concept of SAAG
2 Hepatitis A,B most important, remote infection of hep
b,serology of hept b
Breast/male/female reproductive
1 BRCA 1/her 2 neu etc
2 Klinefelter syndrome
Derma Pathology
1 Immunofluorescence of pemphigus vulgaris
2 Molluscum contagiosum