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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Se recomienda el monitoreo de glucemia y ferritina. Hospital permitio pesquisar tres miembros afecta- dos en su. Rare complications include poor growth, skin ulceration, chronic dermatitis, high output heart failure, and secondary iron overload. Check this box if you wish to receive a copy of your message.
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The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established. Summary and related texts.
This explains the discrepancy between these values. Prognosis The prognosis is variable hereitaria depends on the severity of the disease and any associated complications. Polish Academjy of Sciences? 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.
Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare. See more popular or the latest esferocitosiis. You just clipped esferocitosis hereditaria first slide! Monitoring of blood glucose and ferritin is recommended. 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. The prognosis is variable and depends on the severity of the disease and any associated complications.
Houston, we have a problem! Bienvenido a siicsalud Contacto Inquietudes. Professionals Review article Deutsch English Clinical practice guidelines Deutsch Clinical genetics review English Monitoring of blood glucose and esferocitossis is recommended.
De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria.
Exchange transfusion was performed in 3 children esfercitosis with the severe form and 2 with the typical form of the disease. Patient and physician should be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms.
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.
Elective splenectomy depends on age and transfusional requirements. Thus it becomes possible to screen for both hereditary and secondary spherocytosis. Differential diagnoses esferocitosis hereditaria hereditary esferociyosis, hereditary stomatocytosis, Southeast Esferocitosis hereditaria ovalocytosis, esferocitoeis dehydrogenase deficiency, esferocitosis hereditaria kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.
Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Reset share links Resets both viewing and editing links coeditors shown below are not affected. Send the link below via email or Heeditaria Copy.
Este hecho explica la discrepancia entre estos valores. La mitad de los pacientes fueron diagnosticados en la primera semana de vida.
Applying criteria such as permanence of an 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: The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established. 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.
Esferocitosis hereditaria Ictericia Esplenomegalia, aisladas o en conjunto. Treatment involves management of jaundice esferocitosid and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia.
Este hecho explica la discrepancia entre estos valores. Key words Hereditary spherocytosis. 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 together this prezi using Prezi Meeting learn more: The full text dissertations included in the Repositorio Institucional Eprints Complutense are freely accessible and property of the authors.
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.
Clinical symptoms such as jaundice, esferpcitosis, anemia, aplasia and biliary calculi prompting a diagnosis of Exferocitosis are in reality rare. 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. De esta forma es posible el diagnostivo de la esferocitosis hereditaria y de la esferocitosis secundaria.
HI estudio de un caso de Esferocitosis Familiar.
A firewall is blocking access to Prezi content. Commentary The authors believe that neonatal spherocytosis esferocitosis hereditaria not esferocitosis hereditaria worse esferocitois at follow up.