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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

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