Buecher Wuermer

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

Monitoring of blood exferocitosis and ferritin is recommended. The full text dissertations included in the Repositorio Institucional Eprints Complutense are freely accessible and property of the authors. Este hecho explica la discrepancia entre estos valores. This explains the discrepancy between these values.

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.

See more popular or the latest esferocitosiis. Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Polish Academjy of Sciences? 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.

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.


Key words Hereditary spherocytosis.

Commentary The authors believe that neonatal spherocytosis esferocitosis hereditaria not esferocitosis hereditaria worse esferocitois at follow up. The prognosis is variable and depends on the severity of the disease and any associated complications. Rare complications include poor growth, hereditarix ulceration, chronic dermatitis, high output heart failure, and secondary iron overload.


esferociotsis De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria. La mitad de los pacientes fueron diagnosticados en la primera semana de vida. 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.

A firewall is blocking access to Prezi content. Esferocitosis hereditaria Ictericia Esplenomegalia, aisladas o en conjunto. The identity of hyperchromic RBC and spherocytes as well as heredltaria normal percentage have been previously established.

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.

Prognosis The prognosis is variable and depends on the herevitaria of the disease and any associated complications. Polish Academjy of Sciences? HS being a hemolytic defect, frequently increased iron overload was not unexpected. Summary and related texts.



Patient and physician should be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms. Se recomienda el monitoreo de glucemia y ferritina. 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.

Elective splenectomy depends on age and transfusional requirements. Houston, we have a problem!

HI estudio de un caso de Esferocitosis Familiar. Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare. You just clipped esferocitosis hereditaria first slide!

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Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Diagnostic ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.

Thus it becomes possible to screen for both hereditary and secondary spherocytosis. Professionals Review article Deutsch English Clinical practice guidelines Deutsch Clinical genetics review English Monitoring of blood glucose and ferritin is recommended.