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An Unusual Case of Pancytopenia With Hepatosplenomegaly Case Report

2023-01-06

Abstract excerpt

BACKGROUND Gaucher’s disease is one of the most common lysosomal storage diseases characterized by hematologic abnormalities, organomegaly, and skeletal involvement. It is caused by reduced activity of the enzyme acid β-glucosidase which is encoded by a gene on chromosome 1q21-q31 1 . There are 3 clinical subtypes distinguished by the presence or absence and progression of neurologic manifestations: type 1 or the...

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Literature Corpus work
61b50fac-fece-5503-862e-221a843b2916
DOI
10.21203/rs.3.rs-1407435/v1
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