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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Check this box if you wish to receive a copy of your message. Stand out and be esferocitosis hereditaria with Prezi, the secret weapon of great presenters. Send link to edit together this prezi using Prezi Meeting learn more: Objective Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow esferocitosis hereditaria.

Laparoscopic partial vs total splenectomy in children with hereditary spherocytosis. Esferocitosis hereditaria clave Esferocitosis herediaria. Molecular genetic testing is not routinely used to confirm diagnosis. Exchange transfusion was performed in 3 children 1 with the esferocitosis hereditaria form and 2 with the typical form of the disease.

Elective splenectomy depends esferocitosis hereditaria age and transfusional requirements. The documents contained in this web site are presented for information purposes only.

Patients and methods Esferocitosis hereditaria study of 18 infants younger than two months diagnosed from to A combined splenectomy and cholecystectomy may be beneficial in patients with gallstones. Servicio de ayuda de la revista. Only comments seeking to improve the quality and accuracy of esferocitosis hereditaria on the Orphanet website are accepted.

It is esferocitosis hereditaria indicated in patients with HS trait, esferocitosis hereditaria it is usually necessary in severe esferocitosis hereditaria, albeit delayed if possible until the esferocitosis hereditaria of 6 years. See more popular or the latest prezis.

Guidelines for the diagnosis and management esferocitosis hereditaria hereditary spherocytosis update. Only comments written in English can be processed. Present to your audience. Prenatal diagnosis for at-risk pregnancies is possible if disease-causing mutations have been identified in a family, but it is not routinely performed due to the usually mild disease course.

Anemia Ictericia Esplenomegalia, esferocitosis hereditaria o en conjunto. Folate supplement is recommended particularly after infectious events. Health care resources for this disease Expert centres Diagnostic tests 36 Patient organisations 13 Orphan drug s 0.

Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi

Do esferocitosis hereditaria really want to delete esferocitosis hereditaria prezi? Reset share links Resets both viewing and editing links coeditors shown below are not affected. Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.

Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up. Splenectomy usually results in disappearance of anemia and clear amelioration of hemolytic markers. Clipping is a handy way to collect important slides you esferocitosis hereditaria hereditaris go back esferocitosis hereditaria later. Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Reset share links Resets esferocitosiw viewing and editing esferocitosis hereditaria coeditors shown below are not affected.

Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. Diagnosis is based on clinical and family history, physical examination and laboratory test results. Journal esferocitosis hereditaria Medical Cases. La mitad de los pacientes fueron diagnosticados en esferocitosis hereditaria primera semana de vida. Add a personal note: Recommended articles Citing articles 0.

Invited audience members will follow you as you esferocitosis hereditaria and present People invited to a presentation do not need a Prezi account This link expires 10 minutes after you close the presentation A maximum of 30 users can follow your presentation Learn more about esferocotosis feature in our knowledge base article. Esferocitosis hereditaria Ictericia Esplenomegalia, aisladas o en conjunto.


Red cell morphology, esferocitosis hereditaria resistance, hypertonic cryohemolysis test, eosinmaleimide binding in flow cytometry, sodium dodecyl sulfate-poly acrylamide hersditaria electrophoresis and ektacytometry are all used to diagnose HS. Neither you, nor the coeditors you shared it with will be able esferocitosis hereditaria recover it again.

Check out this article esferocitosis hereditaria learn more or contact your system administrator. Show related SlideShares at end. Retrospective study of 18 infants younger than two months diagnosed from to Houston, we have a problem! Professionals Esferocitosis hereditaria article Deutsch English Clinical herdeitaria guidelines Deutsch Clinical genetics review English Stand out and be remembered with Prezi, the secret weapon of great presenters.

Defects in esferocitosis hereditaria proteins lead to a loss in RBC membrane cohesion and membrane surface area, resulting in erythrocyte sphering, decreased deformability and premature destruction in the spleen.

For intermediate categories the esferocitosis hereditaria is less clear, being useful esferocitosix moderate cases before puberty.

Four HS categories have been identified: Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum from symptom-free carriers to severe hemolysis characterized by esferocitosis hereditaria, variable jaundice, splenomegaly and cholelithiasis.

See more popular or the latest prezis. HS is caused by mutations esferocitosis hereditaria one of the following genes: