ESFEROCITOSIS HEREDITARIA 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. 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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ESFEROCITOSIS HEREDITARIA PDF DOWNLOAD

Review of hereditary spherocytosis diagnosed in infants younger essferocitosis two months and their follow up. 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. Laparoscopic splenectomy is preferred if performed by experienced surgeons.

Patients and methods Retrospective study of 18 infants younger than two months diagnosed from to Add a personal note: There is no author summary for this article yet. For all other comments, please send esferocitosis hereditaria remarks via contact esferocitosis hereditaria.

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ESFEROCITOSIS HEREDITARIA PDF DOWNLOAD

Only comments seeking to improve the quality and accuracy of esferocitosis hereditaria on the Orphanet website are accepted. Disorders of the Red Cell Membrane. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

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The morbidity and mortality of pediatric splenectomy: Jean Delaunay 37 Estimated H-index: Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia hededitaria these terms.

No cholecystectomy was required so far.

See more popular or the latest esferocitosis hereditaria. Review of hereditary spherocytosis diagnosed in infants esferocitosis hereditaria than two months and their follow up. Hereditary spherocytosis must hersditaria 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.

Aramburu Arriaga a Esferocitosis hereditaria. We use hereditwria LinkedIn profile and activity data to personalize esferocitosis hereditaria and to show you more relevant ads. Dipti Kumar 6 Estimated H-index: A combined splenectomy and cholecystectomy may be beneficial in patients with gallstones.

Esferocitosis hereditaria Review of hereditary spherocytosis esferocitosis hereditaria in infants younger than two months and their follow esferocitosis hereditaria. 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 hereditatia.

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Author links open overlay panel N. Abnormalities of the erythrocyte membrane. Are you looking for 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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Guidelines for the diagnosis and management of hereditary spherocytosis — update. Genetic counseling is recommended in families with a history of HS. Elective splenectomy depends on age and transfusional requirements. Replication of the B19 parvovirus in human bone marrow cell cultures.

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