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Gaucher Disease: An Underdiagnosed Pathology in the Eastern Moroccan Population
Gaucher disease (GD) is a lysosomal storage disease. It corresponds to a congenital deficit in β-glucocerebrosidase. This pathology should be considered in the presence of unexplained splenomegaly, with or without signs of haemorrhage, skeletal manifestations or hepatomegaly. The diagnosis is based...
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| Gepubliceerd in: | EJIFCC |
|---|---|
| Hoofdauteurs: | , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
The Communications and Publications Division (CPD) of the IFCC
2019
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6416808/ https://ncbi.nlm.nih.gov/pubmed/30881277 |
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