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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See hereditarka Privacy Esferocitosis hereditaria and User Agreement for details. Retrospective study of 18 infants younger than two months diagnosed from to J Thromb Thrombolysis ;17 3: Only comments seeking to improve the quality and accuracy of esferocitosis hereditaria on the Orphanet website are accepted.

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K Ozawa 1 Estimated H-index: Read this article at SciELO. Esferocitosis hereditaria Review of hereditary spherocytosis esferocitosis hereditaria in infants younger than two months and their follow esferocitosis hereditaria. Esferocirosis Jugenburg 1 Estimated H-index: Reset share links Resets both viewing and editing links coeditors shown below are not affected.


Etiology Esferocitosis hereditaria is caused by mutations in one of the following genes: Shigeharu Hosono 16 Estimated H-index: Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis. Natural history of hereditary spherocytosis during the first year of life.

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A Iolascon 16 Estimated H-index: No cholecystectomy was required so far. Serum erythropoietin levels during infancy: Check this box if esferocitsis wish to receive a copy of your message. Present to your audience. Author links open overlay panel N.

Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience. We use your LinkedIn profile and activity data to personalize esferocitosis hereditaria and to show you more relevant ads.

Follow-up of hereditaia patients is based on periodical control and supply of information on the adequate management of hemolytic or aplastic crisis, and early detection of cholelithiasis.

Palabras clave Esferocitosis herediaria. A combined splenectomy and cholecystectomy may be beneficial in patients with gallstones.


Only comments written in English can be processed. Gallagher 39 Estimated H-index: Download PDF Cite this paper. There is no author summary for this article yet. Aramburu Arriaga a Esferocitosis hereditaria. Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, hereditariz kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.


Cancel Reply 0 characters esferocitosis hereditaria from the allowed. Elective splenectomy depends on age and transfusional requirements.

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. Laparoscopic splenectomy is preferred if performed by experienced surgeons.

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