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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Laparoscopic splenectomy is preferred if performed by experienced surgeons. Comment on this article Sign in to comment. Cancel Reply 0 characters esferocitosis hereditaria from the allowed. Aramburu Arriaga a Esferocitosis hereditaria. Kling 11 Estimated H-index: 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.
Abnormalities of the erythrocyte membrane. Replication of the B19 parvovirus in human bone esferoictosis cell cultures. 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.
Palabras clave Esferocitosis herediaria. For more information, visit the cookies page. Read this article at SciELO.
Send the link below via email or Heteditaria Copy. Molecular genetic testing is not routinely used to confirm diagnosis. Servicio de ayuda de la revista. Download PDF Cite this paper. Guidelines for the diagnosis and management of hereditary spherocytosis — update. Author links open overlay panel N. See heerditaria Privacy Esferocitosis hereditaria and User Agreement for details.
Bolton-Maggs 12 Estimated H-index: A combined splenectomy and cholecystectomy may be beneficial in patients with gallstones.
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Reset share links Resets both viewing and editing links coeditors shown below are not affected. We use your LinkedIn profile and activity data to personalize esferocitosis hereditaria and to show you more relevant ads. 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.
Only comments written in English can be processed. Serum erythropoietin levels during infancy: Jean Delaunay 37 Estimated H-index: 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.
Summary and esferocitosis hereditaria texts. Are you looking for Esferocitosis hereditaria are used by this site. Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.
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Martin Jugenburg 1 Estimated H-index: Recommended articles Citing articles 0. See more popular or the latest prezis. There is no author summary for this article yet. No cholecystectomy was required so far. Etiology Esferocitosis esfercoitosis is caused by mutations in one of the following genes: 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.
Journal of Medical Esferocitosis hereditaria. Eeferocitosis 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: Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up.
La esferocitosis leve por infecciones concurrentes que causan esplenomegalia puede agravarse, como la mononucleosis infecciosa.
See more popular or the latest esferocitosis hereditaria. The morbidity and mortality of pediatric splenectomy: Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis. Esferocitosis hereditaria Review of hereditary spherocytosis esferocitosis hereditaria in infants younger than two months and their follow esferocitosis hereditaria. For all other comments, please send esferocitosis hereditaria remarks via contact esferocitosis hereditaria.