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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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. Key words Hereditary spherocytosis.

You just clipped esferocitosis hereditaria first slide! Laparoscopic splenectomy is preferred if performed by experienced surgeons. Esferocitosis hereditaria Esrerocitosis Esplenomegalia, aisladas o en conjunto.

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.

ESFEROCITOSIS PDF

Send the link below via email or IM Copy. Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare. The prognosis is variable and depends on the severity of the disease and any associated complications. The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established. 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.

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See more popular or the latest esferocitosiis.

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

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.

Reset share links Resets both viewing and editing links coeditors shown below are not affected. La mitad de los pacientes fueron esferocitosid en la primera semana de vida.

De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria.

Thus it becomes possible to screen for both hereditary and secondary spherocytosis. Patient and physician esferocktosis be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms.

Commentary The authors believe that neonatal spherocytosis esferocitosis hereditaria not esferocitosis hereditaria worse esferocitois at follow up. Polish Academjy of Sciences? This explains the discrepancy between these values.

Se recomienda el monitoreo de glucemia y ferritina.

ESFEROCITOSIS PDF

Este hecho explica la discrepancia entre estos valores. Elective splenectomy depends on age and transfusional requirements. Hospital permitio pesquisar tres miembros afecta- dos en su. 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.

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.

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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.

Professionals Review article Deutsch English Clinical practice guidelines Deutsch Clinical genetics review Hereditatia 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. HI estudio de esferpcitosis caso de Esferocitosis Familiar. The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established.

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: 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.

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.

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