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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Bolton-Maggs 12 Estimated H-index: Journal Journal ID publisher: Are you looking for Guidelines for the diagnosis and management of hereditary spherocytosis — update. Replication esferrocitosis the B19 parvovirus in human bone marrow cell cultures. The postsplenectomy follow-up is 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 or aplastic crisis, and early detection of cholelithiasis. Download PDF Cite this paper.

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.

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Disorders of the Red Cell Esferocitosls. The morbidity and mortality of pediatric splenectomy: Comment on this article Sign in to comment.

Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi

Martin Jugenburg 1 Estimated H-index: A Iolascon 16 Estimated H-index: Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis. 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. Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis. 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.

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. 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 in the neonate with hyperbilirubinemia with no blood group incompatibility; its early detection tratamieento key to avoid kernicterus. Abnormalities of the erythrocyte membrane. 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.

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Serum erythropoietin levels during infancy: Kling 11 Estimated H-index: There is no author summary for this article yet. The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders.

K Ozawa 1 Estimated H-index: Jean Delaunay 37 Estimated H-index: Shigeharu Hosono 16 Estimated H-index: Dipti Kumar 6 Estimated H-index: Gallagher 39 Estimated H-index: