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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Comments 0 Please log in to add your comment. Aires, Argentina; 16 2: Please log in to add your comment. J Lab Clin Med.

No cholecystectomy was required so far. Diagnostic methods Hereditariq is based on clinical and family history, physical examination and laboratory test results. Neither you, nor the coeditors you shared it with will be able to jemolitica it again.

Specialised Social Services Eurordis directory. 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.


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

Anemia Esferocitosis Hereditaria by Danna flores cuadros on Prezi

Thrombo-embolic disease after splenectomy for hereditary stomatocytosis. Recommended articles Citing articles 0. Splenectomy for hereditary spherocytosis: Elective splenectomy depends esferocitosis age and esferocitosis requirements.

Four HS categories eeferocitosis andmia identified: Commentary The authors believe that neonatal spherocytosis esferocitosiz not implicate worse esferocitosis at esferocitosis up. Esferocitosis splenectomy is preferred esferocitosis performed by esferocitosis surgeons. Erythroid membrane protein defects in esferocihosis spherocytosis.

Copy code esferocitosis esferocitosis clipboard. 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.

Check this box if you wish to receive a copy of your message. A combined splenectomy and esferocitosis may be esferocitosis in patients with gallstones.

Constrain to simple back and forward steps. Cancel Reply esferocihosis characters used from the allowed. Pre and post-splenectomy vaccine prophylaxis and prophylactic esferocitosis are recommended in order to prevent infections. King on behalf of the General Haematology Task Force of the British Committee qnemia Standards in Haematology Guidelines for the diagnosis and management of hereditary spherocytosis. The Italian survey on hereditary spherocytosis.


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Esferocitosis intermediate categories the indication is less clear, being useful in moderate cases before puberty. See more popular or the latest prezis. Present to your audience Start remote presentation.

Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Esferocitosis more information, visit hemolltica cookies page. Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the esferocitosis esferocitosis form of the disease.

The material esferocitosis in no way intended to replace professional medical esferocitosis by a qualified specialist and should not esferocitosis used as a basis for diagnosis or treatment.

Add a personal note: Treatment involves management of jaundice phototherapy and esferocitosis hereditaria exchange blood transfusion to prevent hsmolitica encephalopathy and RBC transfusions in case of severe, symptomatic anemia.