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Púrpura Trombocitopénica Imune na Criança Casuística do Serviço de Hematologia ...
Pina, Francisca; Lobo, Isabel; Pinho, M. J.; Benedito, Manuela; Maricato, M. L.; Tamagnini, G.autores apresentam uma revisão de 196 casos clínicos de crianças a quem foi diagnosticada Púrpura Trombocitopénica Imune (PTI) no períodocompreendido antre 1977 e 1993, e seguidas na consulta externa de Hematologia do Hospital Pediátrico.Questionam, dado o carácter benigno da doença, a obrigatoriedade da execução de medulograma e a necessidade de tratamento.Concluem que o grupo etário mais afectado foi o das cr...
Severe hereditary spherocytosis and distal renal tubular acidosis associated wi...
Ribeiro, ML; Alliosio, N; Almeida, H; Gomes, C; Texier, P; Lemos, C; Mimoso, G; Morlé, L; Bey-Cabet, F; Rudigoz, RC; Delaunay, J; Tamagnini, GAbsence of band 3, associated with the mutation Coimbra (V488M) in the homozygous state, caused severe hereditary spherocytosis in a young child. Although prenatal testing was made available to the parents, it was declined. Because the fetus stopped moving near term, an emergency cesarean section was performed and a severely anemic, hydropic female baby was delivered. She was resuscitated and initially kept ali...
Type-II dyserythropoietic anemia. A partial form of the glycoprotein degradatio...
Marques, J M; Serviço de Pediatria e Neonatologia, Hospital Central Conde de S. Januário, Macau.; Tamagnini, G; Humberto, JThe authors present a case of a boy, aged 8 years and 11 months, yellow race, with dyserythropoietic anemia type II, diagnosed at two months of age. Screening for partial form of carbohydrate deficient glycoprotein syndrome was normal. This result did not confirm the publication by Fukuda in 1990. ; The authors present a case of a boy, aged 8 years and 11 months, yellow race, with dyserythropoietic anemia type...
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