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 tratamifnto 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. The morbidity and mortality of pediatric splenectomy: Serum erythropoietin levels during infancy: Dipti Kumar 6 Estimated H-index: Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis.

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Jean Delaunay 37 Estimated H-index: Self URI journal page: 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. Abnormalities of the erythrocyte membrane.

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Martin Jugenburg 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. Bolton-Maggs 12 Estimated H-index: Shigeharu Hosono 16 Estimated H-index: Download PDF Cite this paper.

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K Ozawa 1 Estimated H-index: Kling 11 Estimated H-index: Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis. There is no author summary tratamienfo this article yet.

The esferrocitosis follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders. Natural history of hereditary spherocytosis during the first year of life.

Disorders of the Red Cell Membrane. Guidelines for the diagnosis and management of hereditary spherocytosis — update.

Read this article at SciELO. 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: A Iolascon 16 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.

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Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi

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. 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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