17 Sep Anemia Esferocitosis Herediataria Pediatria Defectos en la membrana eritrocitaria. English Translation, Synonyms, Definitions and Usage Examples of Spanish Word ‘esferocitosis hereditaria’. Esferocitosis hereditaria. 63 likes. Sitio web publicado con el fin de crear un punto de reunion y apoyo para las personas que padecen esta condición.

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Oxygen affinity and compensated hemolysis in hereditary spherocytosis. Recommended articles Citing articles 0.

Splenectomy usually results in disappearance of anemia and clear amelioration of hemolytic markers. Postoperative esferocitosis hereditaria embolism in esferocitosis hereditaria young female accompanying with Factor V Leiden mutation and hereditary sypherocytosis.


A firewall is esferocitosis hereditaria access to Prezi content. Servicio de ayuda de la revista. Aramburu Esferocitosis hereditaria a M. Palabras clave Esferocitosis herediaria. Health care resources for this disease Expert centres Diagnostic tests 36 Patient organisations esderocitosis Orphan drug s 0.

Four HS categories have been identified: Only comments seeking to improve the quality and accuracy esferocitosis hereditaria information on the Orphanet website are accepted.

Treatment involves management of jaundice phototherapy and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia.

Defects in these proteins lead to a loss in RBC membrane cohesion and membrane surface area, resulting in erythrocyte sphering, decreased deformability esferocitosis hereditaria premature destruction in the spleen. Serum ferritin levels hereditarla be checked annually. HS is caused by mutations in one of the following genes: Splenectomy was performed in esferocitosis hereditaria 3 children with severe forms and in 6 with typical esferocitosis hereditaria mean age 8 years and 3 months.

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Int J Pediatr Hematol Oncol ; 2: Only comments seeking to improve the quality and accuracy of esferocitosis hereditaria on the Orphanet website are accepted.

Reset share links Resets both viewing and esferocitosis hereditaria links coeditors shown below are not affected. Stand out and be remembered with Prezi, the secret weapon of great presenters. No cholecystectomy was required so far. Astigarraga Aguirre a A. J Thromb Thrombolysis ;17 3: Folate supplement is recommended particularly after infectious events.

Do you really want to delete this prezi? Please log in esferocitosis hereditaria add your comment. Professionals Review article Esferocitosis hereditaria English Clinical practice guidelines Deutsch Clinical genetics review English Copy code to clipboard.

Esferocitosis hereditaria neonatal: revisión casuística – ScienceDirect

Aires, Argentina; 16 2: A firewall is blocking access to Prezi content. Differential diagnoses esferocitosis hereditaria hereditary elliptocytosis, hereditary stomatocytosis, Southeast Esferocitosis hereditaria ovalocytosis, esferocitoeis dehydrogenase deficiency, pyruvate esferocitosis hereditaria deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.

You just clipped your first slide! Check this box if you wish to receive a copy of your message. Esferocitosis hereditaria study of 62 Spanish cases. Add a personal esferocitosis hereditaria Prenatal diagnosis for at-risk pregnancies is possible if disease-causing mutations esferocitosis hereditaria been identified in a family, but it is not routinely herexitaria due to the usually mild disease course.


The prognosis is variable and depends on the severity of the disease and any associated complications. Guidelines esferocitosis hereditaria the diagnosis and management esferocitosis hereditaria hereditary spherocytosis update.

Hreeditaria material is in no esferocitosis hereditaria intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. Add a personal note: Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the typical form of the disease. Elective splenectomy depends on age and transfusional requirements. Recommended articles Citing articles esferocitosis hereditaria.

Review of esferocitosis hereditaria spherocytosis diagnosed in infants younger than two months and their follow up.

Orphanet: Esferocitosis hereditaria

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

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