Neurology
Rheumatology
Dermatology
Endocrinology
Genetics
100

Also known as alarm clock headache

Hypnic headache

100

Shawl sign is seen in which condition

Dermatomyositis

100

Location of most aggressive squamous cell carcinoma lesions

lips

100

Hormonal tests done in patients with asymptomatic adrenal incidentaloma are for these conditions

pheochromocytoma, subclinical cushings syndrome

100

Role of genetic variation on response to a drug

Pharmacogenomics

200

DOC for treatment of fatigue on MS

Modafinil
200

Recombinant uricase enzyme used to treat severe or refractory gout

Pegloticase

200

1- 3 mm papule seen on faces and chest of HIV patients

Eosinophilic folliculitis

200

Best single test for acromegaly

serum igf-1 concentration

200

Name of a genetic test to identify asymptomatic individuals for a heterozygous disorder

Carrier testing

300

DOC for treatment of non traumatic aneurysmal SAH

nimodipine

300

Antibody involved in immune mediated necrotizing myopathy

Anti HMGCOA reductase antibody

300

DOC for treatment of chronic cutaneous SLE

Hydroxychloroquine

300

Preferred diagnostic test for patients with elevated PTH and serum calcium but very low urinary calcium excretion

Calcium/creatinine clearance ratio

300

Segment of chromosome that shortens with aging

Telomeres

400

NMDA encephalitis is associated with which cancer

Ovarian teratomas

400

Eponym for retroperitoneal fibrosis

Ormond disease

400

Name of condition

Acne Keliodalis nuchae

400

3 antibodies present in type 1 DM

Anti GAD 65, 1A-2, Islet cell antibodies, zinc transporter 8 antibodies

400

Term for alteration of chromosome gene expression without changing the nucleotide base sequence

Epigenetic change

500

Eponym for vertebro-basilar insufficiency

Beauty parlor syndrome

500

Antibody associated with scleroderma renal crises

Anti RNA polymerase iii

500

Zinc deficiency is associated with this skin condition

acrodermatitis enteropathica

500

Syndrome for DI, DM, optic atrophy and deafness

Wolfram syndrome

500

Likelihood of developing a disease when the disease causing genetic mutation is present

Penetrance