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ChapterBiochemistry Lysosomal storage diseases

Diagnostic approaches

Free notes, MCQs, tables & flowcharts for USMLE Step 3 Biochemistry

10Questions
10Flashcards
1Tables & Flowcharts

Sample Questions

1

You examine an infant in your office. On exam you observe hypotonia, as well as the findings shown in Figures A and B. You order laboratory testing, which demonstrates the findings shown in Figure C. Which of the following is the most likely pathologic mechanism involved?

AAccumulation of galactocerebroside

BAccumulation of ceramide trihexoside

CAccumulation of GM2 ganglioside

DAccumulation of glucocerebroside

EAccumulation of sphingomyelin

2

A 7-month-old boy is brought by his parents to the pediatrician’s office. His mother says the child has been weakening progressively and is not as active as he used to be when he was born. His condition seems to be getting worse, especially over the last month. He was born at 41 weeks through normal vaginal delivery. There were no complications observed during the prenatal period. He was progressing well over the 1st few months and achieving the appropriate milestones. On examination, his abdomen appears soft with no liver enlargement. The patient appears to be dehydrated and lethargic. The results of a fundoscopic examination are shown in the picture. A blood test for which of the following enzymes is the next best assay to evaluate this patient's health?

AAcid alpha-glucosidase

BHexosaminidase

CSphingomyelinase

DGlucocerebrosidase

EArylsulfatase A

3

A deficiency in which of the following lysosomal enzymes is inherited in a pattern similar to a deficiency of iduronate sulfatase (Hunter syndrome)?

ASphingomyelinase

BGlucocerebrosidase

CGalactocerebrosidase

DAlpha-L-iduronidase

EAlpha-galactosidase A

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