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Esferocitosis hereditaria. Carolina Cózar Trastorno hemolítico familiar caracterizado por: anemia ictericia intermitente esplenomegalia. Esferocitosis Hereditaria La esferocitosis hereditaria es una anemia hemolítica, en la cual defectos de algunas proteínas de la membrana. Esferocitosis hereditaria. Revisión. Parte II. Manifestaciones clínicas, evolución, complicaciones y tratamiento. PUBLISHED | A. Posadas.

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Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience. Self URI journal page: Kling 11 Estimated H-index: Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis.

Journal Journal ID publisher: Bolton-Maggs 12 Estimated H-index: Hereditary spherocytosis must always be suspected in children with anemia, hyperbilirubinem ia, splenomegaly or cholelithiasis, in the asymptomatic esfferocitosis with an affected relative, and in the neonate with hyperbilirubinemia with no blood group incompatibility; its early detection is key to avoid kernicterus.

K Ozawa 1 Estimated H-index: Follow-up of these patients is based on periodical control and supply of information on the adequate management of hemolytic or aplastic crisis, and early detection of cholelithiasis. Shigeharu Hosono 16 Estimated H-index: Gallagher 39 Estimated H-index: The decision to perform splenectomy is usually associated with quality of life rather than life-threatening risk, and it should result from a consensus between patient, parents and physicians.

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Follow-up of these patients is based on periodical control and supply of information on the adequate management of hemolytic or aplastic crisis, and early detection of cholelithiasis. Jean Delaunay 37 Estimated H-index: Download PDF Cite this paper. Are you looking for Read this article at SciELO. Dipti Kumar 6 Estimated H-index: There is no author summary for this article yet.

A Iolascon 16 Estimated H-index: Replication of the B19 parvovirus in human bone marrow cell cultures.

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Disorders of the Red Cell Membrane. Hereditary spherocytosis must always be suspected in children with anemia, hyperbilirubinemia, splenomegaly or cholelithiasis, in the asymptomatic individual with an affected relative, and in the neonate with hyperbilirubinemia with no blood group incompatibility; its early detection is key to avoid kernicterus.

The morbidity and mortality of pediatric splenectomy: The decision to perform splenectomy is usually associated with quality of life rather than life-threatening risk, and it should result from a consensus between patient, parents and physicians. The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders.

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The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders.

Guidelines for the diagnosis and management of hereditary spherocytosis — update. Natural history of hereditary spherocytosis during the first year of life.

Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis. Serum erythropoietin levels during infancy: Comment on this article Sign in tratamirnto comment. Martin Jugenburg 1 Estimated H-index: Abnormalities of the erythrocyte membrane.