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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Detalles Bibliográficos
Autores principales: Bouayadi, Ouardia, Lyagoubi, Amina, Aarab, Adnane, Lamrabat, Somiya, Berhili, Abdelilah, Bensalah, Mohammed, Seddik, Rachid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Communications and Publications Division (CPD) of the IFCC 2019
Materias:
Discussion
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6416808/
https://www.ncbi.nlm.nih.gov/pubmed/30881277

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6416808/
https://www.ncbi.nlm.nih.gov/pubmed/30881277

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