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Hemoglobin D-beta (0) thalassemia. A case report and family study.
Dawod, S T; Abulaban, M; Kamel, K; Huisman, T H.
Afiliação
  • Dawod ST; Department of Pediatrics, Hamad General Hospital, Qatar, Arabian Gulf.
Am J Pediatr Hematol Oncol ; 10(4): 316-8, 1988.
Article em En | MEDLINE | ID: mdl-3239708
Findings are presented on a Pakistani family in Doha, Qatar with hemoglobin D-Los Angeles (alpha 2 beta 3 121 (glutamine----glycine) and thalassemia trait. The propositus, a child, has hemoglobin D-beta(0) thalassemia, and suffers from moderately severe hemolytic anemia. The father has beta-thalassemia trait, and the mother is heterozygous for hemoglobin D-Los Angeles. This, the eighth confirmed case in the medical literature, is reported to emphasize its clinical manifestations and genetic basis.
Assuntos
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Base de dados: MEDLINE Assunto principal: Talassemia / Hemoglobinas Anormais Limite: Humans / Infant / Male País como assunto: Asia Idioma: En Ano de publicação: 1988 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Talassemia / Hemoglobinas Anormais Limite: Humans / Infant / Male País como assunto: Asia Idioma: En Ano de publicação: 1988 Tipo de documento: Article