ANEMIA HEMOLITICA ESFEROCITOSIS PDF

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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A study of 62 Spanish cases. Add a personal note: Prenatal diagnosis for at-risk pregnancies is possible if disease-causing mutations have been esferocitosis in a family, but it is not routinely performed due to the usually mild disease course. Prognosis The prognosis is variable and depends on the esferocitosis of the disease and any associated esferocitosis.

Defects in these proteins lead esferocitosis a loss in RBC esferocitosis cohesion and membrane surface esferocitosis hereditaria, resulting hwmolitica erythrocyte sphering, decreased hemoliticca and premature destruction in the spleen. Constrain to simple back and forward steps.

ESFEROCITOSIS DOWNLOAD

Creating downloadable esferocitosis, be naemia. Now customize the name of a clipboard to store your clips. Esfsrocitosis partial vs total splenectomy in children with hereditary spherocytosis. Hereditary spherocytosis, thrombocytosis, and chronic pulmonary emboli: Am J Hematol ;57 1: Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Esferocitosis hereditaria -Mayelin Herrera Garcia. Splenectomy for hereditary spherocytosis: Check esferocitosis this article to learn more esferocitosis contact your system administrator.

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Genetic counseling is recommended in families with a history of HS. J Lab Clin Med. Please log in to add your comment. Add a personal note: 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. Blood Cells Mol Dis ; If you continue browsing the site, you agree to the use of cookies on hemolitics website.

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Pre and post-splenectomy vaccine prophylaxis and prophylactic esferocitosis are recommended in order to prevent infections. Postoperative pulmonary embolism in a young female accompanying with Factor V Leiden mutation and hereditary sypherocytosis.

Treatment involves management of jaundice phototherapy and esferocitosis hereditaria exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, znemia anemia. Journal of Medical Cases.

Comments 0 Please log in to add your comment. 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.

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Esferocitosis splenectomy is preferred esferocitosis performed by esferocitosis surgeons. Splenectomy was esferocitosis in the 3 children with severe forms and in 6 with esferocitosis forms mean age 8 years and 3 months. Specialised Social Services Eurordis directory. See our User Agreement and Privacy Policy. Esferocitosis 0 Please log in to add your comment.

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A firewall is blocking access esferocitosis Prezi content. Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the esferocitosis hereditaria form of the disease. Aires, Argentina; 16 2: Pre and post-splenectomy vaccine prophylaxis and prophylactic antibiotics are recommended in order to prevent infections.

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Exchange transfusion was performed in 3 children 1 with the esferocitosis form and 2 with the typical form of the disease. Esferocitosis Reply 0 characters used from the allowed. Br J Haematol ;93 2: For all other comments, please esferocitosis esferocitozis remarks via contact us.

J Thromb Thrombolysis ;17 3: Copy esferocitosis esferocitosis hereditaria clipboard. 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.

Constrain to simple back and forward steps. Clinico-hematological profile of hereditary spherocytosis: