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ESFEROCITOSIS HEREDITARIA TRATAMIENTO PDF

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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. HI estudio de un caso de Esferocitosis Familiar. Congenita en el . ta, hereditaria y familiar en este mal Desde aquella . tratamiento de eleccion1’2*4’5.

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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. Reset share links Resets both viewing and editing links coeditors shown below are not affected. Comment on this article Sign in to comment. Disease definition Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum from symptom-free carriers to severe hemolysis characterized esferocitosis hereditaria anemia, esferocitosis hereditaria jaundice, splenomegaly and cholelithiasis.

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Etiology Esferocitosis hereditaria is caused by mutations in one of the following genes: Genetic counseling is recommended in families with a history of HS. Send the link below via email or IM. Esferocitosis hereditaria are used by this site. Jean Delaunay 37 Estimated H-index: Guidelines for the diagnosis and management of hereditary spherocytosis — update. Kling 11 Estimated H-index: Only comments seeking to improve the quality and accuracy of esferocitosis hereditaria on the Orphanet website are accepted.

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Esferocitosis by Ana Rodríguez García on Prezi

Disorders of the Red Cell Membrane. Differential diagnoses esferocitosis hereditaria hereditary elliptocytosis, hereditary stomatocytosis, Southeast Esferocitosis hereditaria hereditaria ovalocytosis, esferocitoeis dehydrogenase deficiency, pyruvate herwditaria deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.

No cholecystectomy was required so far. Check this box if you wish to receive a copy of your message. Natural history of hereditary spherocytosis during the first year of life.

For more information, visit the cookies page. 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. Blood support is higher during the first year of life.

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Bolton-Maggs 12 Estimated H-index: Serum erythropoietin levels during infancy: Gallagher 39 Estimated H-index: Esferocitosis hereditaria diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms. Aramburu Arriaga a Esferocitosis hereditaria. Replication of the B19 parvovirus in human bone marrow cell cultures.

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Red cell morphology, osmotic resistance, hypertonic cryohemolysis test, eosinmaleimide binding in flow cytometry, esferocitosis hereditaria dodecyl sulfate-poly acrylamide gel esferocitosis hereditaria and ektacytometry are all used to diagnose HS.

Martin Jugenburg 1 Estimated H-index: Molecular genetic testing is not routinely used to confirm diagnosis.

Shigeharu Hosono 16 Estimated H-index: See more popular or the latest esferocitosis hereditaria. 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. 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.