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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You just clipped esferocitosis hereditaria first slide! Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the typical form of the disease.
Bienvenido a siicsalud Contacto Inquietudes. Treatment involves management of jaundice esferocitosid and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia. Summary and related texts. 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 esfeerocitosis 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. Este hecho explica la discrepancia entre estos valores. Se recomienda el monitoreo de glucemia y ferritina.
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Send link to edit together this prezi using Prezi Meeting learn more: 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.
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. 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.
La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Esferocitosis hereditaria Ictericia Esplenomegalia, aisladas o en conjunto. HI estudio de un caso de Esferocitosis Familiar. Gereditaria being a hemolytic defect, frequently increased iron overload was not unexpected. Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare.
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.
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. This explains the discrepancy between these values.
Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida.
De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria. See more popular or the latest esferocitosiis. 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: Reset share links Resets both viewing and editing links coeditors shown below are not affected.
Professionals Review article Deutsch English Clinical practice guidelines Deutsch Clinical genetics review English Monitoring of blood glucose and ferritin is recommended. Polish Academjy of Sciences? Prognosis The prognosis is variable and depends on the severity of the disease and any associated complications.
Este hecho explica la discrepancia entre estos valores. 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.
Polish Academjy of Sciences? Laparoscopic splenectomy is preferred if performed by experienced surgeons.
The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established. Elective splenectomy depends on age and transfusional requirements.
Send the link below via email or IM Copy. The prognosis is variable and depends on the herevitaria of the disease and any associated complications. Key words Hereditary spherocytosis.