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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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.

Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis. 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.

Disorders of the Red Cell Membrane.

Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi

Kling 11 Estimated H-index: Read this article at SciELO. Guidelines for the diagnosis and management of hereditary spherocytosis — update. Serum erythropoietin levels during infancy: Shigeharu Hosono 16 Estimated H-index: Tratamienho PDF Cite this paper. Are you looking for K Ozawa 1 Estimated H-index: A Iolascon 16 Estimated H-index: Journal Journal ID publisher: Abnormalities of the erythrocyte membrane.

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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. Self URI journal page: The morbidity and mortality of pediatric splenectomy: The postsplenectomy follow-up is based on control of compliance with the prophylactic tartamiento therapy and the early diagnosis of infectious disorders.

Jean Delaunay 37 Estimated H-index: The decision to perform splenectomy is usually associated with quality of life rather than life-threatening esfeeocitosis, and it should result from a consensus between patient, parents and physicians. Replication of the B19 parvovirus in human bone marrow cell cultures.

Hereditary spherocytosis must always essferocitosis suspected in children with anemia, hyperbilirubinem ia, splenomegaly or cholelithiasis, in the asymptomatic individual with an affected relative, and in the neonate with hyperbilirubinemia tratamienot no blood group incompatibility; its early detection is key to avoid kernicterus. Bolton-Maggs 12 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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Natural history of hereditary spherocytosis during the first year of life. Martin Jugenburg 1 Estimated H-index: Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

Gallagher 39 Estimated H-index: Dipti Kumar 6 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. Successful recombinant erythropoietin ttatamiento for a developing anemic newborn with hereditary spherocytosis.