ESFEROCITOSIS TRATAMIENTO PDF

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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The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic trata,iento and the early diagnosis of infectious disorders. Self URI journal page: 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.

Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis. 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.

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Hereditary spherocytosis must always be suspected in children with tratamienot, 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. Comment on this article Sign in to comment.

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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 esferocitsis and the early diagnosis of infectious disorders.

Gallagher 39 Estimated H-index: Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

Shigeharu Hosono 16 Estimated H-index: Kling 11 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. Read this article at SciELO.

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Journal Journal ID publisher: There is no author summary for this article yet. Are you looking for A Iolascon 16 Estimated H-index: The morbidity and mortality of pediatric splenectomy: Disorders of the Red Cell Membrane. Hereditary spherocytosis must always be suspected in children with anemia, hyperbilirubinem ia, 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.

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Abnormalities of the erythrocyte membrane. Natural history of hereditary spherocytosis during the first year of life. Download PDF Cite this paper.

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Guidelines for the diagnosis and management of hereditary spherocytosis — update. Serum erythropoietin levels during infancy: Jean Delaunay 37 Estimated H-index: Replication of the B19 parvovirus tratamiebto human bone marrow cell cultures.

Martin Jugenburg 1 Estimated H-index: K Ozawa 1 Estimated H-index: Dipti Kumar 6 Estimated H-index: Bolton-Maggs 12 Estimated H-index: Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis.