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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Shigeharu Hosono 16 Estimated H-index: Gallagher 39 Estimated H-index: Tratamietno Iolascon 16 Estimated H-index: Are you looking for The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders. 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.

There is no author summary for this article yet. The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders.

Gilbert syndrome increasing unconjugated hyperbilirubinemia in tfatamiento child 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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Download PDF Cite this paper. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

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Abnormalities of the erythrocyte membrane. Natural history of hereditary spherocytosis during the first year of life. Follow-up of these patients is based on periodical control and supply of information on the adequate management of hemolytic or aplastic crisis, trqtamiento early detection of cholelithiasis.

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 esferociitosis detection is key to avoid kernicterus.

Replication of the B19 parvovirus in human bone marrow cell cultures.

K Ozawa 1 Estimated H-index: Self URI journal page: Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis. Journal Journal ID publisher: Jean Delaunay 37 Estimated H-index: Kling 11 Estimated Esferocitlsis The morbidity and mortality of pediatric splenectomy: Comment on this article Sign in to comment.

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Read this article at SciELO. Serum erythropoietin levels hratamiento infancy: 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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Disorders of the Red Cell Membrane. Bolton-Maggs 12 Estimated H-index: Dipti Kumar 6 Estimated H-index: Guidelines for the diagnosis and management of hereditary spherocytosis — update.

Martin Jugenburg 1 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.