mtDNA Deletion in an Iranian Infant with Pearson Marrow Syndrome

BACKGROUND: Pearson syndrome (PS) is a rare multisystem mitochondrial disorder of hematopoietic system, characterized by refractory sideroblastic anemia, pancytopenia, exocrine pancreatic insufficiency, and variable neurologic, hepatic, renal, and endocrine failure. CASE PRESENTATION: We describe a...

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Detalhes bibliográficos
Main Authors: Arzanian, Mohammad Taghi, Eghbali, Aziz, Karimzade, Parvaneh, Ahmadi, Mitra, Houshmand, Massoud, Rezaei, Nima
Formato: Artigo
Idioma:Inglês
Publicado em: Tehran University of Medical Sciences 2010
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3445998/
https://ncbi.nlm.nih.gov/pubmed/23056691
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