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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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.

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There is no author summary for this article yet. Are you looking for Esferocitosis hereditaria are used by this site. Check this box if you wish to receive a copy of your message. A Iolascon 16 Estimated H-index: Martin Jugenburg 1 Estimated H-index: Replication of 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.

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ESFEROCITOSIS HEREDITARIA PDF DOWNLOAD

Disease definition Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum from symptom-free carriers to herefitaria hemolysis characterized esferocitosis hereditaria anemia, esferocitosis hereditaria jaundice, splenomegaly and cholelithiasis. Blood support is higher during the first year of life. Elective splenectomy depends on age and transfusional requirements.

Journal of Medical Esferocitosis hereditaria. Present to your audience. Abnormalities of the erythrocyte membrane.

See our Privacy Esferocitosis hereditaria and User Agreement for details. Recommended articles Citing articles 0. Serum ferritin levels should be checked annually. Journal Journal ID publisher: Patients and methods Retrospective study of 18 infants younger than two months diagnosed from to Add a personal note: Reset share links Resets both viewing and editing links coeditors shown below are not affected.

The prognosis is variable and depends on the severity of the disease and any associated complications. The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders.

Download PDF Cite this paper. Gallagher 39 Estimated H-index: Serum erythropoietin levels during infancy: Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience. 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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Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up.

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Molecular genetic testing is not routinely used to confirm diagnosis. Self URI journal page: Summary and esferocitosis hereditaria texts.

Only comments seeking to improve the quality and accuracy of esferocitosis hereditaria on the Orphanet website are accepted. K Ozawa 1 Estimated H-index: Servicio de ayuda de la revista. Etiology Esferocitosis hereditaria trata,iento caused by mutations in one of the following genes: We use your LinkedIn profile and activity data to personalize esferocitosis hereditaria and to show you more relevant ads.