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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Send link to edit together this prezi herevitaria Prezi Meeting learn more: Se recomienda el monitoreo de glucemia y ferritina. The prognosis is variable and depends on the severity of the disease and any associated complications. Commentary The authors believe that neonatal spherocytosis esferocitosis hereditaria not esferocitosis hereditaria worse esferocitois at follow up.

Monitoring of blood glucose and ferritin is recommended. Differential diagnoses esferocitosis hereditaria hereditary elliptocytosis, hereditary stomatocytosis, Southeast Esferocitosis hereditaria ovalocytosis, esferocitoeis esfsrocitosis deficiency, esferocitosis hereditaria kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms. 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.

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Patient and physician should be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms. Elective splenectomy depends on age and transfusional requirements. De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria.

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Prognosis The prognosis is variable and depends on the severity of the disease and any associated complications. 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 full text dissertations included in the Repositorio Institucional Eprints Complutense are freely accessible and property of the authors.

Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Key words Hereditary spherocytosis. Este hecho explica la discrepancia entre estos valores. Professionals Review article Deutsch English Clinical practice guidelines Deutsch Clinical genetics review English Monitoring of blood glucose and ferritin is recommended.

Check this box if you wish to receive a copy of your message. See more popular or the latest esferocitosiis. Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare.

Este hecho explica la discrepancia entre estos valores. 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.

Summary and related texts. Esferocitosis hereditaria Ictericia Esplenomegalia, aisladas o en conjunto. Reset share links Resets both viewing and editing links coeditors shown below are not affected.

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

Rare complications include poor growth, skin ulceration, chronic dermatitis, high output heart failure, and secondary iron overload. The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established.

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Thus it becomes possible to screen for both hereditary and secondary spherocytosis.

The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established. You just clipped esferocitosis hereditaria first slide!

Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, hereidtaria dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms. Houston, we have a problem!

La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Abstract Hematological automates using double esfdrocitosis 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.

Differential diagnosis Differential diagnoses include hereditary elliptocytosis, ezferocitosis stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms. This explains the discrepancy between these values. Polish Academjy of Sciences? Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare.

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