An infant with Pearson syndrome: a rare cause of congenital sideroblastic anemia and bone marrow failure

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Bibliographische Detailangaben
Veröffentlicht in:	Blood 2017-05, Vol.129 (19), p.2710-2710
Hauptverfasser:	Falcon, Corey P., Howard, Thomas H.
Format:	Artikel
Sprache:	eng
Schlagworte:	Acyl-CoA Dehydrogenase, Long-Chain - deficiency Acyl-CoA Dehydrogenase, Long-Chain - genetics Acyl-CoA Dehydrogenase, Long-Chain - metabolism Anemia, Sideroblastic - complications Anemia, Sideroblastic - genetics Anemia, Sideroblastic - metabolism Anemia, Sideroblastic - pathology Bone Marrow - metabolism Bone Marrow - pathology Bone Marrow Diseases - complications Bone Marrow Diseases - genetics Bone Marrow Diseases - metabolism Bone Marrow Diseases - pathology Congenital Bone Marrow Failure Syndromes Humans Infant Lipid Metabolism, Inborn Errors - complications Lipid Metabolism, Inborn Errors - genetics Lipid Metabolism, Inborn Errors - metabolism Lipid Metabolism, Inborn Errors - pathology Male Mitochondrial Diseases - complications Mitochondrial Diseases - genetics Mitochondrial Diseases - metabolism Mitochondrial Diseases - pathology Muscular Diseases - complications Muscular Diseases - genetics Muscular Diseases - metabolism Muscular Diseases - pathology
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