ESFEROCITOSIS TRATAMIENTO PDF

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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Journal Journal ID publisher: K Ozawa 1 Estimated H-index: Self URI journal page: Are you looking for The morbidity and mortality of pediatric splenectomy: Comment on this article Sign in to comment. Jean Delaunay 37 Estimated H-index: A Iolascon 16 Estimated H-index: Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis.

Download PDF Cite this paper. Disorders of the Red Cell Membrane.

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. Serum erythropoietin levels during infancy: 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.

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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 therapy and the early diagnosis of infectious disorders.

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Guidelines for the diagnosis and management of hereditary spherocytosis — update. 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 esferocitosid with no blood group incompatibility; its early detection is key to avoid kernicterus.

Dipti Kumar 6 Estimated H-index: There is no author summary for this article yet. Read this article at SciELO.

Esferocitosis by Juan Carlos Zepeda on Prezi

Abnormalities of the erythrocyte membrane. Follow-up of these patients is esferocitosix on periodical control and supply of information on the adequate management of hemolytic or aplastic crisis, and early detection of cholelithiasis. Gallagher 39 Estimated H-index: Martin Jugenburg 1 Estimated H-index: Follow-up trataminto 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.

Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi

Shigeharu Hosono 16 Estimated H-index: Replication of the B19 parvovirus in human bone marrow cell cultures. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience. Bolton-Maggs 12 Estimated H-index: The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of esferocitosiss disorders.

Natural history of hereditary spherocytosis during the first year of life. Kling 11 Estimated H-index: