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Gaucher Disease for Hematologists

Gaucher disease (GD) is a rare hereditary lysosomal storage disease that arises due to deficiency of glucocerebrosidase. Early diagnosis is very important for starting proper treatment and preventing complications. Splenomegaly, anemia, and thrombocytopenia are the most common findings in GD and so...

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Principais autores: Gül Nihal Özdemir, Eren Gündüz
Format: Artigo
Sprog:Inglês
Udgivet: Turkish Society of Hematology 2022-05-01
Serier:Turkish Journal of Hematology
Fag:
gaucher disease
anemia
thrombocytopenia
splenomegaly
Online adgang:https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tjh&un=TJH-89983
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