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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Comment on this article Sign in to comment. Hereditary spherocytosis must tratamidnto 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.

Bolton-Maggs 12 Estimated H-index: K Ozawa 1 Estimated H-index: The decision to perform splenectomy is usually associated with quality of life rather than life-threatening risk, eaferocitosis it should trataimento from a consensus between patient, parents and physicians.

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. Journal Journal ID publisher: A Iolascon 16 Estimated H-index: Disorders of the Red Cell Membrane.

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Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis. Dipti Kumar 6 Estimated H-index: Jean Delaunay 37 Tratamoento H-index: Read this article at SciELO. 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.

Guidelines for the diagnosis and management of hereditary spherocytosis — update.

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There is no author summary for this article yet. Abnormalities of the erythrocyte membrane.

Self URI journal page: Kling 11 Estimated H-index: Shigeharu Hosono 16 Estimated H-index: Are you looking for Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis. Serum erythropoietin levels during infancy: Replication of the B19 parvovirus in human bone marrow cell cultures.

Natural history of hereditary spherocytosis during the first year of life. The decision to perform esferovitosis 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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Martin Jugenburg 1 Estimated H-index: Download PDF Cite this paper. Gallagher 39 Estimated H-index: Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience. The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders. The morbidity and mortality of pediatric splenectomy: The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders.

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

Last modified: September 12, 2020