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Congenital dyserythropoietic anemia type II associated with G6PD Seattle in a Sicilian child.
Gangarossa, S; Romano, V; Miraglia del Giudice, E; Perrotta, S; Iolascon, A; Schiliro, G.
Afiliação
  • Gangarossa S; Divisione di Ematologia-Oncologia Pediatrica, Università di Catania, Italia.
Acta Haematol ; 93(1): 36-9, 1995.
Article em En | MEDLINE | ID: mdl-7725848
ABSTRACT
A 2-year-old Sicilian boy was investigated because of chronic nonspherocytic hemolytic anemia (CNSHA) associated with hepatosplenomegaly. Appropriate studies revealed deficiency of glucose-6-phosphate dehydrogenase type Seattle (G6PD Seattle). In addition, bone marrow morphology, serological studies and analysis of red cell membrane proteins revealed congenital dyserythropoietic anemia (CDA) type II (or HEMPAS). Because G6PD Seattle on its own does not cause CNSHA, we believe that the clinical manifestations in this patient are essentially due to the CDA type II abnormality. However, the coexistence of these two different red cell abnormalities may affect the clinical picture specifically by making CDA type II more hemolytic than it would have been otherwise.
Assuntos
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Base de dados: MEDLINE Assunto principal: Deficiência de Glucosefosfato Desidrogenase / Anemia Diseritropoética Congênita / Anemia Hemolítica Congênita não Esferocítica Idioma: En Ano de publicação: 1995 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Deficiência de Glucosefosfato Desidrogenase / Anemia Diseritropoética Congênita / Anemia Hemolítica Congênita não Esferocítica Idioma: En Ano de publicação: 1995 Tipo de documento: Article