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Unexpected Cause of Persistent Microcytosis and Neurological Symptoms in a Child: Niemann-Pick Disease Type C.
Cervera Bravo, Aurea; Osuna Marco, Marta P; Morán-Jiménez, María-José; Martín-Hernández, Elena.
Afiliação
  • Cervera Bravo A; Department of Pediatrics, Móstoles University Hospital, Móstoles.
  • Osuna Marco MP; Department of Pediatric Hematology and Oncology, Montepríncipe HM Hospital, Boadilla del Monte.
  • Morán-Jiménez MJ; Instituto de Investigación Sanitaria (Health Research Institute) of the 12 de Octubre University Hospital (imas12), Section 3: Rare Diseases, Group: Porphyrias, Hemochromatosis and Anemias.
  • Martín-Hernández E; Unit of Hereditary Mitochondrial & Metabolic Diseases, Department of Pediatrics, 12 de Octubre University Hospital, National Reference Center for Hereditary Metabolic Diseases (C.S.U.R.) and European Reference Network for Hereditary Metabolic Disorders (MetabERN), Madrid, Spain.
J Pediatr Hematol Oncol ; 43(8): e1238-e1240, 2021 Nov 01.
Article em En | MEDLINE | ID: mdl-33661177
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Niemann-Pick Tipo C / Transtornos do Neurodesenvolvimento / Anemia Hipocrômica / Ferro Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Niemann-Pick Tipo C / Transtornos do Neurodesenvolvimento / Anemia Hipocrômica / Ferro Idioma: En Ano de publicação: 2021 Tipo de documento: Article