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Beta Thalassemia Major with Gaucher’s Disease: A Rare Entity

Thalassemia is a genetic disorder due to deletion or mutation in the gene for alpha or beta chain of hemoglobin. Gaucher’s disease (GD) is characterized by a deficiency of a lysosomal enzyme, glucocerebrosidase which occurs due to mutations in the GBA1 gene on chromosome 1. Thalassemia and GD have o...

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Detalles Bibliográficos
Autores principales:	Bai, Naila, Nasir, Sharmeen, Ahmed, Jawad, Malik, Farheen, Bin Arif, Taha
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Cureus 2019
Materias:	Endocrinology/Diabetes/Metabolism
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6758988/ https://www.ncbi.nlm.nih.gov/pubmed/31565589 http://dx.doi.org/10.7759/cureus.5179

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