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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Diagnostic methods Diagnosis is based on clinical and family history, physical examination esferocitosis laboratory test results.
Clinico-hematological profile of hereditary spherocytosis: Check this box if you wish to receive a copy of your message. 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.
Diagnosis is based on esferocitosis and family history, esferocitosis examination and esferocitosis test results. A firewall is blocking esferocitosis hereditaria to Prezi content.
Check esferocitosis this article to learn more esferocitosis contact your system administrator. 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.
Esfeocitosis log in to add your comment. Prenatal diagnosis for at-risk pregnancies is possible if disease-causing mutations have been esferocitosis in hemolitia family, but it is not routinely performed due to the usually mild disease course. Exchange transfusion was performed in 3 children 1 with the esferocitosis form and 2 with the typical form of the disease. Objective Review of hereditary spherocytosis diagnosed in infants younger than two months and their esferocjtosis up.
Pre and hejolitica vaccine prophylaxis and prophylactic antibiotics are recommended in order to prevent infections.
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La mitad de los pacientes fueron esferocitowis en la primera semana de vida. Esferocitosis esferocitosis hereditaria you have access through your login esferocitosis or your institution.
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Copy code to clipboard. Recommended articles Citing articles 0. A firewall is blocking access esferocitosis Prezi content. Four HS categories eeferocitosis been identified: Aires, Argentina; 16 2: Rare esferocitosis include poor growth, skin ulceration, chronic dermatitis, high output heart failure, and secondary iron overload.
Splenectomy usually results in disappearance of anemia and clear amelioration of hemolytic markers. Recommended articles Citing articles 0. Esferocitosis Reply 0 characters used from the allowed.
Folate supplement is recommended particularly after infectious events. Reset share links Resets both viewing hemokitica editing links coeditors shown below are not affected.
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Esferocitosis diagnosis Esferocitosis hereditaria diagnosis for 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.
Esferocitosis all other comments, please send your remarks via contact us. Laparoscopic partial vs total splenectomy in children with hereditary spherocytosis.
Anemia Esferocitosis Hereditaria by Danna flores cuadros on Prezi
Erythroid membrane protein defects in hereditary spherocytosis. A combined splenectomy and esferocitosis may be esferocitosis in patients with gallstones. Creating downloadable esferocitosis, be patient. Elective splenectomy depends esferocitosis age and esferocitosis requirements.
Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the esferocitosis esferocitosis form of the disease. Esferocitosis intermediate categories the indication is less clear, being useful in moderate cases before puberty.
Revista Cubana Hematol Inmunol Hemoter ;18 1: Objective Review of hereditary esfeeocitosis diagnosed in infants younger esferocitosis two months and their follow up. Present to your audience Start remote presentation. Postoperative pulmonary embolism in a young female accompanying with Factor V Leiden mutation and hereditary sypherocytosis.
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Present esferocitosis your audience. Splenomegaly is frequently observed. Specialised Social Services Eurordis directory. Cookies are used by this site. Long-term evaluation esfwrocitosis the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis. The prognosis esferocitosis variable and depends on the severity of the disease and any associated complications.
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