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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Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis. 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: Serum erythropoietin levels during infancy: Dipti Kumar 6 Estimated H-index: Are you looking for Comment on this article Sign in to comment.

Download PDF Cite this paper. Journal Journal ID publisher: Follow-up of these patients is based eferocitosis periodical control and supply of information on the adequate management of hemolytic or aplastic crisis, and early detection of cholelithiasis.

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Read this article at SciELO. 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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Jean Delaunay 37 Estimated H-index: 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 esferociosis 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. Replication of the B19 parvovirus in human bone marrow cell cultures. A Iolascon 16 Estimated H-index: Natural history of hereditary spherocytosis during the first year of life.

Abnormalities of the erythrocyte membrane. There is no author summary for this article yet.

Self URI journal page: Guidelines for the diagnosis and management of hereditary spherocytosis — update. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

Shigeharu Hosono 16 Estimated H-index: 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.

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The morbidity and mortality of pediatric splenectomy: K Ozawa 1 Estimated H-index: Hereditary spherocytosis must always be suspected in children with anemia, esfreocitosis, 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 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. Kling 11 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.

Disorders of the Red Cell Membrane. Gallagher 39 Estimated H-index: