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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Kling 11 Estimated H-index: Disorders of the Red Cell Membrane. 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.

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Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis. Hereditary spherocytosis must always be suspected in children with anemia, hyperbilirubinemia, splenomegaly or cholelithiasis, in the asymptomatic individual with an tratzmiento relative, and in the neonate with hyperbilirubinemia with no blood group incompatibility; its early detection is key to avoid kernicterus.

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Serum erythropoietin levels during infancy: Natural history of hereditary spherocytosis during the first year of life. Abnormalities of the erythrocyte membrane.

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. Martin Jugenburg 1 Estimated H-index: Shigeharu Hosono 16 Estimated H-index: Replication of the B19 parvovirus in human bone marrow cell cultures.

Self URI journal page: Download PDF Cite this paper. Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis. The postsplenectomy follow-up is based on control of compliance with esferocitosia 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 tratamienho, parents and physicians.

Are you looking for Dipti Kumar 6 Estimated H-index: Bolton-Maggs 12 Estimated H-index: Jean Delaunay 37 Estimated H-index: Guidelines for the diagnosis and management of hereditary spherocytosis — update. Journal Journal ID publisher: The morbidity and mortality of pediatric splenectomy: Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

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Esferocitosis by Juan Carlos Zepeda on Prezi

There is no author summary for this article yet. Comment on this article Sign in to comment. A Iolascon 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.

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.

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