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

MeSH terms

• 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 Diseases* / complications
• Bone Marrow Diseases* / genetics
• Bone Marrow Diseases* / metabolism
• Bone Marrow Diseases* / pathology
• Bone Marrow* / metabolism
• Bone Marrow* / 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