Pitfalls in the diagnosis of Gaucher disease in Iraq: A diagnostic experience from a developing country

BACKGROUND AND OBJECTIVES: Gaucher disease (GD) is a rare hereditary disorder caused by deficiency of the lysosomal enzyme β-glucocerebrosidase. An early and definitive diagnosis minimizes the sequelae of misdiagnoses, and unnecessary and invasive diagnostic procedures. METHODS: A cross-sectional de...

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Detalles Bibliográficos
Autores principales: Thejeal, Rabab Farhan, wahhab, Saja Baheer Abdul, Saadi, Nebal Waill
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Professional Medical Publications 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155412/
https://www.ncbi.nlm.nih.gov/pubmed/34104165
http://dx.doi.org/10.12669/pjms.37.3.2930

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8155412/
https://www.ncbi.nlm.nih.gov/pubmed/34104165
http://dx.doi.org/10.12669/pjms.37.3.2930

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