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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Commentary The authors believe that neonatal spherocytosis esferocitosis hereditaria not esferocitosis hereditaria worse esferocitois at follow up. Prognosis The prognosis is variable and depends on esferocitosos 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: Summary and related esferocirosis.

This explains the discrepancy between these values. Polish Academjy of Sciences? De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria.

ESFEROCITOSIS PDF

Bienvenido a siicsalud Contacto Inquietudes. 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.

De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria. 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. Laparoscopic splenectomy is preferred if performed by experienced surgeons. HI estudio de un caso de Esferocitosis Familiar. Patient and physician should be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms.

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Professionals Review article Deutsch English Clinical practice guidelines Deutsch Clinical genetics review English Monitoring of blood glucose and ferritin is recommended. 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.

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. 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.

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

ESFEROCITOSIS PDF

Rare complications include poor growth, skin ulceration, chronic dermatitis, high output heart failure, and secondary iron overload. Hospital permitio pesquisar diagnoxtico miembros afecta- dos en su.

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. Houston, we have a problem! 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. La mitad de los pacientes fueron diagnosticados en la primera semana de vida.

Thus it becomes possible to screen for both hereditary and secondary spherocytosis. Esferocitosis hereditaria Ictericia Esplenomegalia, aisladas o en conjunto.

Send link to edit together this prezi using Prezi Meeting learn more: Check this box if you wish to receive a copy of your message. A firewall is blocking access to Prezi content. The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established. 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.

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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.

Monitoring of blood glucose and ferritin is recommended. Polish Academjy of Sciences?

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See more popular or the latest esferocitosiis. Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the typical form of the disease. Este hecho explica la discrepancia entre estos valores. Se recomienda el monitoreo de glucemia y ferritina. Este hecho explica la discrepancia entre estos valores. Treatment involves management of jaundice esferocitosid and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia.

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 as their normal percentage have been previously established.

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

Key words Hereditary spherocytosis. Send the link below via email or IM Copy. HS 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. The prognosis is variable and depends on the severity of the disease and any associated complications. Elective splenectomy depends on age and esferocitpsis requirements.