Chapter·PsychiatryGenetic and Metabolic Disorders

Lysosomal Storage DiseasesDownloads

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Sample Questions

1

A child presents with bone pain and hepatosplenomegaly, indicative of Gaucher's disease. A trephine biopsy and aspirate show the following finding. Which of the following is the most likely enzyme deficient in this condition?

AHexosaminidase

BGlucocerebrosidase

CSphingomyelinase

DAlpha 1,4-glucosidase

2

Which one of the following diseases is classified as an autosomal dominant disorder?

AHemochromatosis

BPhenylketonuria

CMaturity onset diabetes of the young

DGlucose-6 phosphate dehydrogenase deficiency

3

A patient presents with an X-ray showing cardiomegaly, along with symptoms of hypotonia, macroglossia, hepatomegaly, and floppy baby syndrome. The X ray of the infant is shown below. What is the most likely diagnosis?

APompe's disease

BEbstein anomaly

CTransposition of great arteries

DVon Gierke's disease

ECongenital hypothyroidism

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