Accepted
at 4:18 a.m. Nov, 01, 2023
by
Ahmed7
Author:
shmuelsash
Type of change:
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Hepatosplenomegaly, pancytopenia, bone pain / fractures, failure to thrive, and delayed puberty are features characteristic of {{c1::Gaucher disease::genetic condition}}
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Due to accumulation of glucocerebroside in macrophages of bone marrow (anemia / thrombocytopenia), spleen, liver, and bones
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Sketchy



Watch Biochemistry Sphingolipidoses: Gaucher Disease, Metachromatic Leukodystrophy, and Krabbe Disease
Watch Pediatric Sphingolipidoses: Gaucher Disease, Metachromatic Leukodystrophy, and Krabbe Disease



Watch Biochemistry Sphingolipidoses: Gaucher Disease, Metachromatic Leukodystrophy, and Krabbe Disease
Watch Pediatric Sphingolipidoses: Gaucher Disease, Metachromatic Leukodystrophy, and Krabbe Disease
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