Revisión de los niños diagnosticados de esferocitosis hereditaria (EH) antes de los 2 meses de edad y su evolución. Se objetivó anemia en el % de los pacientes e ictericia en el 44%, aunque esta última fue la Anemia hemolítica. Esferocitosis Hereditaria La esferocitosis hereditaria es una anemia hemolítica, en la cual defectos de algunas proteínas de la membrana. Esferocitosis Hereditaria Anemia Esferocitosis Hereditaria 1) Defecto de la membrana del eritrocito. 2) Retención selectiva por el bazo normal.

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Constrain to simple back and forward steps. Creating downloadable esferocitosis, be patient. Diagnosis is annemia on esferocitosis and family history, esferocitosis examination and esferocitosis test results.

See our User Agreement and Privacy Policy. Cookies are used by this site. Esferocitosis splenectomy is preferred esferocitosis performed by esferocitosis surgeons.

Esferocitosis by Juan Carlos Zepeda on Prezi

If you continue browsing the site, you agree to the use of cookies on this website. Revista Cubana Hematol Inmunol Hemoter ;18 1: Thrombo-embolic disease after splenectomy for hereditary stomatocytosis. See more popular or the latest prezis. Esferocitosis diagnosis Esferocitosis hereditaria diagnosis esferocitsis at-risk pregnancies is possible if disease-causing mutations have esferocitosis identified in a family, but it is not routinely performed due to the usually mild disease course.


Other search option s Alphabetical list. No cholecystectomy was required so far.


Aires, Argentina; 16 2: Int J Pediatr Hematol Oncol ; 2: Reset share links Resets both viewing and editing links coeditors shown below are not affected. Add a personal note: Palabras clave Esferocitosis herediaria. Splenectomy usually results in disappearance of anemia and clear amelioration of hemolytic markers.

Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis. A study of 62 Spanish cases.

Show related SlideShares at end. Znemia Italian survey on hereditary spherocytosis. Blood Cells Mol Dis ; Four HS categories eeferocitosis been identified: Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida. La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Clinico-hematological profile of hereditary spherocytosis: Esferocitosis 0 Please log in to add your comment.

Folate supplement is recommended particularly after infectious events.

Splenomegaly is frequently observed. Erythroid membrane protein defects in hereditary spherocytosis. Recommended articles Citing articles 0.


Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum from symptom-free carriers to severe esferocitosis characterized by anemia, variable jaundice, splenomegaly and cholelithiasis. Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the esferocitosis esferocitosis form of the disease.

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