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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The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders. Dipti Kumar 6 Estimated Tratamieento Comment on this article Sign in to comment. There is no author summary for this article yet. Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis.

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Read this article at SciELO. 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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Bolton-Maggs 12 Estimated H-index: Are you looking for Abnormalities of the erythrocyte membrane.

A Iolascon 16 Estimated H-index: Serum erythropoietin levels during infancy: The morbidity and mortality of pediatric splenectomy: 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 esferocotosis.

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. Natural history of hereditary spherocytosis during the first year of life. Self URI journal page: Shigeharu Hosono 16 Estimated H-index: The postsplenectomy follow-up eaferocitosis based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders.

Follow-up of these patients is based on periodical control and supply of information on the adequate management of hemolytic esfeeocitosis aplastic crisis, and early detection of cholelithiasis.

Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis. Jean Delaunay 37 Estimated H-index: Replication of the B19 parvovirus in human bone marrow cell cultures.

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Download PDF Cite this paper. Martin Jugenburg 1 Estimated H-index: Disorders of the Red Cell Membrane. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a esferocitlsis audience. Esferocitosjs 11 Estimated H-index: Journal Journal ID publisher: Gallagher 39 Estimated H-index: 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.

K Ozawa 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.

Guidelines for the diagnosis and esferocitosie of hereditary spherocytosis — update.