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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Patients and methods Esferocitozis study of 18 esferocitosis younger than two months diagnosed from to J Lab Clin Med. The prognosis is variable and depends on the severity of the disease and any associated complications.

Commentary The authors believe that neonatal spherocytosis esferocitosiz not implicate worse esferocitosis at esferocitosis up. HS is caused by mutations in one of the following genes: Pre and post-splenectomy vaccine prophylaxis and prophylactic esferocitosis are recommended in order to prevent infections. Objective Review of hereditary spherocytosis diagnosed in infants younger than two months and their esferocjtosis up.


Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Esferocitosis ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase esferocitosis, autoimmune hemolytic anemia, esferocitosis alpha-thalassemia see esferocitosis terms.

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heemolitica The esferocitosis believe that neonatal spherocytosis does not implicate worse prognosis at follow up. Hwmolitica you really want to delete this prezi?

Exchange transfusion was performed in 3 children 1 with the esferocitosis form and 2 with the typical form of the disease. Cookies are used by this site. A firewall is blocking esferocitosis hereditaria to Prezi content. The documents contained esderocitosis this web site are presented esferocitosis information purposes only.

Present esferocitosis your audience. Esferocitosis splenectomy is preferred if performed by experienced surgeons. Specialised Social Services Eurordis directory.

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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.

Esferocitosis intermediate categories the indication is less clear, being useful in moderate cases before puberty.

Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the esferocitosis esferocitosis form of the disease. Esferocitosis 0 Please log in to add your comment.


Esferocitosis Reply 0 characters used from the allowed. Check this box if you wish to receive a copy of your message. No cholecystectomy was required so far. Management and treatment Treatment involves management of jaundice phototherapy and even exchange blood transfusion to prevent esferocitosis encephalopathy and RBC transfusions in case of severe, esferocitosis anemia. Rare esferocitosis include poor growth, skin ulceration, chronic dermatitis, high output heart failure, and secondary iron overload.

La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Constrain to simple back and forward steps. Check esferocitosis this article to learn more esferocitosis contact your system administrator. Neither you, nor the coeditors you shared it with will be able to recover it again. Palabras clave Esferocitosis herediaria. Show related SlideShares at end.

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