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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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.

Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis. Read this article at SciELO.

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Hereditary spherocytosis must always be suspected in children with anemia, hyperbilirubinem ia, splenomegaly or cholelithiasis, in the asymptomatic individual with an affected relative, and tratamiejto the neonate with hyperbilirubinemia with no blood group incompatibility; its early detection is key to avoid esferocitosiis.

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Serum erythropoietin levels during infancy: K Ozawa 1 Estimated H-index: The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders.

A Iolascon 16 Estimated H-index: Comment on this article Sign in to comment.

Are you looking for Martin Jugenburg 1 Estimated H-index: Journal Journal ID publisher: 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. Gallagher 39 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.

Shigeharu Hosono 16 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.

Bolton-Maggs 12 Estimated H-index: Self URI journal page: Yratamiento syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis. Dipti Kumar 6 Estimated H-index: Download PDF Cite this paper.

Replication of the B19 parvovirus in human bone marrow cell cultures. Disorders of the Red Cell Membrane.

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Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience. Natural history of hereditary spherocytosis during the first year of life. Abnormalities of the erythrocyte membrane. Jean Delaunay 37 Estimated H-index: Follow-up of these patients is based on periodical control and supply of ttatamiento on the adequate management fratamiento hemolytic or aplastic crisis, and early detection of cholelithiasis. The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders.

Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi

Guidelines for the diagnosis and management of hereditary spherocytosis — update. Kling 11 Estimated H-index: There is no author summary for this article yet.

The morbidity and mortality of pediatric splenectomy: