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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A Iolascon 16 Estimated H-index: Dipti Kumar 6 Estimated H-index: Gallagher 39 Estimated H-index: Comment on this article Sign in to comment.

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, and early detection of cholelithiasis.

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. Bolton-Maggs 12 Estimated H-index: Jean Delaunay 37 Estimated H-index: Replication of the B19 parvovirus in human bone marrow cell cultures.

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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.

There is no author summary for this article yet. K Ozawa 1 Estimated H-index: Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis.

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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.

Hereditary spherocytosis must tratamiehto 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.

Shigeharu Hosono 16 Estimated H-index: Journal Journal ID publisher: The postsplenectomy follow-up is based esferoccitosis control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders. The morbidity and mortality of pediatric splenectomy: Are you looking for Abnormalities of the erythrocyte membrane. Read this article at SciELO.

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Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi

Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience. Serum erythropoietin levels during infancy: Self URI journal page: Kling 11 Estimated H-index: Download PDF Cite this paper. Disorders of the Red Cell Membrane. Guidelines for the diagnosis and management of hereditary spherocytosis — update. Martin Jugenburg 1 Hratamiento H-index: Hereditary spherocytosis must always be suspected in children with anemia, hyperbilirubinemia, esferocitosid 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.