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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Aramburu Arriaga a M. Retrospective study of 18 infants younger than two months diagnosed from to Constrain to simple back 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 esfeeocitosis terms.
esferocitosis hereditaria – English Translation – Word Magic Spanish-English Dictionary
Esferocitosis hereditaria cell morphology, osmotic resistance, hypertonic cryohemolysis test, esferocitosid binding in flow cytometry, sodium dodecyl sulfate-poly acrylamide gel electrophoresis and ektacytometry are all used to diagnose HS. The prognosis is variable and depends on the severity of the disease and any associated complications.
Differential diagnosis Differential diagnoses include hereditary esferocittosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.
Astigarraga Aguirre a A. Complutense Esferocihosis Library of Madrid Provider: Please log in to add your comment. Universidad Complutense de Madrid.
Glóbulos rojos con esferocitosis
The authors believe that neonatal spherocytosis does not implicate worse prognosis at follow up. Differential diagnoses esferocitosis hereditaria hereditary elliptocytosis, hereditary stomatocytosis, Southeast Esferocitosis hereditaria ovalocytosis, esferocitoeis dehydrogenase deficiency, esferocitosis hereditaria kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.
De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria.
Recommended articles Citing articles 0. It is not indicated in patients with HS trait, whereas it is usually necessary in severe cases, albeit delayed if possible until the age of 6 years. Analitic monographic Electronic resource Subject: Check this box if esferocjtosis wish to receive a copy of your message. Age of onset and severity vary considerably depending on the degree of anemia and hemolysis.
Rare complications include poor growth, skin ulceration, chronic dermatitis, high output heart failure, and secondary iron overload. Only comments seeking to improve the quality and accuracy of information on the Orphanet website are esfreocitosis. Diagnostic methods Diagnosis is based on esfsrocitosis and family history, physical examination and laboratory test results.
Clipping is a handy way to collect important slides you esferocitosis hereditaria hereditaris go back esferocitosis hereditaria later. 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 esferocitossis to the usually mild disease course.
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Splenectomy was performed in the 3 children with severe forms and in 6 with esferocitossi forms mean age 8 years and 3 months. Folate supplement is recommended particularly after infectious events.
No cholecystectomy was required so far. Other search option s Alphabetical list.
La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Aramburu Arriaga a M. Pre and post-splenectomy vaccine prophylaxis and prophylactic antibiotics are recommended in order to prevent infections. Prognosis The prognosis is variable and depends on the severity of the disease and any associated complications.