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A Rare Case of Hemoglobin E Hemoglobinopathy with Gaucher’s Disease

Hemoglobin (Hb) E mutation is common in north-east part of our country. The natural history of Hb E thalassemia is highly variable. The phenotype, for patients with similar mutations, can range from asymptomatic to transfusion dependent. Our patient presented at 2 years of age with failure to thrive...

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Detalhes bibliográficos
Main Authors: Chatterjee, Tathagata, Dewan, Khushboo, Ganguli, P., Das, Satyaranjan, Sharma, Ajay, Sahni, A. K., Nath, Pramod
Formato: Artigo
Idioma:Inglês
Publicado em: Springer-Verlag 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3636348/
https://ncbi.nlm.nih.gov/pubmed/24426351
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12288-012-0153-z
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