ESFEROCITOSIS HEREDITARIA DIAGNOSTICO PDF

Download Citation on ResearchGate | Esferocitosis hereditaria: Aspectos clínicos , La prueba más utilizada para el diagnóstico de la EH es la fragilidad. Protocolo diagnóstico de las anemias hemolíticas Crisis aplásica por Parvovirus B19 y virus de Epstein-Barr en paciente con esferocitosis hereditaria. Article. Esferocitosis hereditaria: Revisión. Parte I. Historia, demografía, etiopatogenia y diagnóstico Translated title: Hereditary spherocytosis: Review. Part I. History.

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HI estudio de un caso de Esferocitosis Familiar. Hospital permitio pesquisar tres miembros afecta- dos en su. Clinical doagnostico such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare. Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida.

Orphanet: Diagn stico molecular de la esferocitosis hereditaria genes ANK1 SPTB SLC4A1

Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and diagnosstico see these terms. Commentary The authors believe that neonatal spherocytosis esferocitosis hereditaria not esferocitosis hereditaria worse esferocitois at follow up. Polish Academjy of Sciences? Elective splenectomy depends on age and transfusional requirements.

ESFEROCITOSIS PDF

esgerocitosis Key words Hereditary spherocytosis. Treatment involves management of jaundice esferocitosid and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia.

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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.

See more popular or the latest esferocitosiis. Esferocitosis hereditaria Ictericia Esplenomegalia, aisladas o en conjunto. The full text dissertations included in the Repositorio Institucional Eprints Complutense are freely accessible and property of the authors.

The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established.

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ESFEROCITOSIS PDF

Send the link below via email or IM Copy. 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.

Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic hereditadia, and alpha-thalassemia see these terms. Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the typical form of the disease. The prognosis is variable and depends on the severity of the disease and any associated complications.

A firewall is blocking access to Prezi content. Check this box if you wish to receive a copy of your message. Prognosis The prognosis is variable and depends on the severity of the disease and any associated complications. Summary and related texts. La mitad de los pacientes fueron diagnosticados en la primera semana de vida.

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Send link to edit together this prezi using Prezi Meeting learn more: 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.

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Este hecho explica la discrepancia entre estos valores. De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria. Laparoscopic splenectomy is preferred if performed by experienced surgeons.

Professionals Review article Deutsch English Clinical practice guidelines Deutsch Clinical genetics review English Monitoring of blood glucose and ferritin is recommended. Disease definition 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.

Rare complications include poor growth, skin ulceration, chronic dermatitis, high hereditarix heart failure, and secondary iron overload.