Mitochondrial Neurogastrointestinal Encephalomyopathy Treated with Stem Cell Transplantation: A Case Report and Review of Literature

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is a rare autosomal recessive disorder. The mutation in the ECGF1 gene causes severe deficiency of thymidine phosphorylase (TP), which in turn increases thymidine and deoxyuridine in the blood, serum, and tissue. The toxic levels of these...

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Autores principales:	Musthafa Chalikandy Peedikayil, Eje Ingvar Kagevi, Ehab Abufarhaneh, Moeenaldeen Dia Alsayed, Hazzaa Abdulla Alzahrani
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	Wolters Kluwer Medknow Publications 2015-04-01
Colección:	Hematology/Oncology and Stem Cell Therapy
Materias:	mitochondrial neurogastrointestinal encephalomyopathy mngie stem cell transplantation bone marrow transplantation
Acceso en línea:	https://journals.lww.com/10.1016/j.hemonc.2014.12.001
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