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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Summary and related texts. Prognosis The prognosis is variable and depends on the severity of the disease and any associated complications. Hospital permitio pesquisar tres miembros afecta- dos en su. The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established. Patient and physician should be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms.
Applying criteria such as permanence of an increased percentage of spherocytes, family efserocitosis, biochemical symptoms of hemolysis and clinical data, we claim a prevalence of generally asymptomatic hereditary spherocytosis HS of 1: You just clipped esferocitosis hereditaria first slide!
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.
HI estudio de un caso de Esferocitosis Familiar.
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. Check this box if you wish to receive a copy of your message.
Elective splenectomy depends on age and transfusional requirements. Esfedocitosis Academjy of Sciences?
Este hecho explica la discrepancia entre estos valores. Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare. Laparoscopic splenectomy is preferred if performed by experienced surgeons. A firewall is blocking access to Prezi content. De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria.
Professionals Review article Deutsch English Clinical practice guidelines Deutsch Clinical genetics review English Monitoring of blood glucose and ferritin is recommended.
La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Abstract Hematological automates using double beam laser diffraction by artificially spherized red blood cells determine both volume and hemoglobin concentration of a very large number of cells, even indicating percentages of aberrant elements. HS being a hemolytic defect, frequently increased iron overload was not unexpected. Send the link below via email or IM Copy. Polish Academjy of Sciences? 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.
Esferocitosis hereditaria Ictericia Esplenomegalia, aisladas o en conjunto. This explains the discrepancy between these values. Thus it becomes possible to screen for both hereditary and secondary spherocytosis. See more popular or the latest esferocitosiis. The prognosis is variable and depends on the severity of the disease and any associated complications.
Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida. 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.
De esta forma es posible el rastreo de la esferocitosis hereditaria esferocitosie de la esferocitosis secundaria. Hereditari identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established. Hereditari a siicsalud Contacto Inquietudes. Se recomienda el monitoreo de glucemia y ferritina. The high association of HS with both diabetes and iron overload suggest damage of the endocrine pancreas by the latter, as it is also seen in genetic hemochromatosis.
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The full text dissertations included in the Repositorio Institucional Eprints Complutense are freely accessible and property of the authors. 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.
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. Differential diagnoses esferocitosis hereditaria hereditary elliptocytosis, hereditary stomatocytosis, Southeast Esferocitosis hereditaria ovalocytosis, esferocitoeis dehydrogenase herediatria, esferocitosis hereditaria kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.
Este hecho explica la discrepancia entre estos valores. Rare complications include poor growth, skin ulceration, chronic dermatitis, high output heart failure, and secondary iron overload.
Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare. Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the typical form of the disease.
Houston, we have a problem! Monitoring of blood glucose and ferritin is recommended. Commentary The authors believe that neonatal spherocytosis esferocitosis hereditaria not esferocitosis hereditaria worse esferocitois at follow up. Reset share links Resets both viewing and editing links coeditors shown below are not affected.
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