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: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Turkish Society of Hematology
2022-05-01
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| Series: | Turkish Journal of Hematology |
| Assuntos: | |
| Acceso en liña: | https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tjh&un=TJH-89983 |
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