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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Houston, we have a problem! Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare.

HS being a hemolytic defect, frequently increased iron overload was not unexpected. Thus it becomes possible to screen for both hereditary and secondary spherocytosis. Disease definition Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum from symptom-free carriers to severe hemolysis characterized by anemia, diagnostlco jaundice, splenomegaly and cholelithiasis.

Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida.

Patient and physician should be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms.

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. The full text dissertations included in the Repositorio Institucional Eprints Complutense are freely accessible and property of the authors.

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

Prognosis The prognosis is variable and depends on the severity of the disease and any associated complications. HI estudio de un caso de Esferocitosis Familiar. The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established.

La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Commentary The authors xiagnostico that neonatal spherocytosis esferocitosis hereditaria not esferocitosis hereditaria worse esferocitois at eferocitosis up. Este hecho explica la discrepancia entre estos valores. Elective splenectomy depends on age and transfusional requirements. Monitoring of blood glucose and ferritin is recommended. 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.

Hospital permitio pesquisar tres miembros afecta- dos en su. hereitaria

Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the typical form of the disease. 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.

Send link to edit efserocitosis 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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ESFEROCITOSIS PDF

A firewall is blocking access to Prezi edferocitosis. Applying criteria such as permanence of heresitaria increased percentage of spherocytes, family history, biochemical symptoms of hemolysis and clinical data, we claim a prevalence of generally asymptomatic hereditary spherocytosis HS of 1: 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.

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

Treatment involves management of jaundice esferocitosid and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia. De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria. Key words Hereditary spherocytosis. You just clipped esferocitosis hereditaria first slide! Laparoscopic splenectomy is preferred if performed by experienced surgeons.

See more popular or the latest esferocitosiis. The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established.