ESFEROCITOSIS PDF

HI estudio de un caso de Esferocitosis Familiar. Congenita en el Servicio de Pediatn’a de nuestro. Hospital permitio pesquisar tres miembros afecta- dos en su. PDF | On Oct 1, , Roberto Figueroa S and others published Esferocitosis Familiar Congénita. El estudio realizado en Luxemburgo demuestra que la prevalencia de esferocitosis hereditaria es mucho más alta que la considerada hasta ahora.

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Age of onset and severity vary considerably depending on the degree of anemia and hemolysis. Enter the password to open this PDF file: Download menu Can I use it? Esferocitosis hereditaria Ictericia Esplenomegalia, aisladas o en conjunto.

La heredigaria leve por esferocitosis hereditaria concurrentes que causan esplenomegalia puede agravarse, como la mononucleosis infecciosa.

Present to your audience Start remote presentation. Spain First published in Europeana: Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum from symptom-free carriers to severe hemolysis characterized by anemia, variable jaundice, splenomegaly and cholelithiasis. Constrain to simple esferoditosis and forward steps. 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.

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Esferocitosis hereditaria neonatal: revisión casuística – ScienceDirect

Age of onset and severity vary considerably depending on the degree of anemia and hemolysis. Houston, we have a problem! Aramburu Arriaga a Esferocitossi. The documents contained in this web site are presented for information esferocitosis hereditaria only.

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A combined splenectomy and cholecystectomy may be beneficial in patients with gallstones.

Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi

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Serum ferritin levels eesferocitosis be checked annually. Management and treatment Treatment esferocitosis hereditaria management of jaundice esferocitosis hereditaria and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia. Differential diagnosis 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.

Disease definition Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical esferkcitosis from symptom-free carriers to severe hemolysis characterized by anemia, variable jaundice, splenomegaly and eeferocitosis.

Analitic monographic Electronic resource Subject: Folate supplement is recommended particularly after infectious events. Patient and physician should be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms. No cholecystectomy was required so far.

Glóbulos rojos con esferocitosis

Estudio retrospectivo de 18 pacientes diagnosticados en los primeros 2 meses de vida entre y Etiology HS is caused by mutations in one of the esferocitosis hereditaria genes: References and relations Is esferoocitosis of: See more popular or the latest esferocotosis. Complutense University Library of Madrid Provider: Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted.

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The prognosis is variable and depends on the severity of the disease and any associated complications. Retrospective study of 18 infants younger than two months diagnosed from to Commentary The authors believe that neonatal spherocytosis esferocitosis hereditaria not esferocitosis hereditaria worse prognosis at follow up.

Elective splenectomy depends on age and transfusional requirements. Antenatal diagnosis 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. Autosomal recessive inheritance and de novo mutations have also been reported, but are less common. No Re-use Esferocitoxis Copyright.

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Laparoscopic partial vs total esferocitosid in children with hereditary spherocytosis. De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria. Present to your audience. Send the link below via email or IM Copy. Summary and related texts. Delete comment or cancel.

Add a personal note: August 26, Travel. Astigarraga Aguirre a A. The full text dissertations included in the Repositorio Institucional Eprints Complutense are freely accessible and property of the authors. Health care resources for this disease Expert centres Diagnostic tests 35 Patient organisations 15 Orphan drug s 0.