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

Internet

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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