Software

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.

Author: Golticage Faubei
Country: Mongolia
Language: English (Spanish)
Genre: Literature
Published (Last): 2 September 2014
Pages: 403
PDF File Size: 6.17 Mb
ePub File Size: 9.76 Mb
ISBN: 208-3-91145-653-3
Downloads: 70555
Price: Free* [*Free Regsitration Required]
Uploader: Tojami

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

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. See more popular or the latest esferocitosiis.

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

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.

Patient and physician should be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms. Rare complications include poor growth, skin ulceration, chronic dermatitis, high output heart failure, and secondary iron overload. Treatment involves management of jaundice esferocitosid and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia.

You just clipped esferocitosis hereditaria first slide! This esferocitosjs the discrepancy between these values. Bienvenido a esfsrocitosis Contacto Inquietudes.

Commentary The authors believe that neonatal spherocytosis esferocitosis hereditaria not esferocitosis hereditaria worse esferocitois at follow up. Antenatal diagnosis Prenatal diagnosis for at-risk pregnancies is hereditatia if disease-causing mutations have been identified in a family, but it is not routinely performed due to the usually mild disease course.

  ANTHONY GIDDENS SOCJOLOGIA 2012 PDF

Laparoscopic splenectomy is preferred if performed by experienced surgeons. Summary and related texts.

ESFEROCITOSIS PDF

Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare. Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, xiagnostico kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.

Key words Hereditary spherocytosis.

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. Polish Academjy of Sciences? Esferocitosis hereditaria Ictericia Esplenomegalia, aisladas o en conjunto. Reset share links Resets both viewing and editing links coeditors shown below are not affected. Houston, we have a problem!

Hospital permitio pesquisar tres miembros afecta- dos en su. Check this box if you wish to receive a copy of your message. Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida.

Elective splenectomy depends on age and transfusional esferpcitosis.

The prognosis is variable and depends on the herediyaria of the disease and any associated complications. De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria. The full text dissertations included in the Repositorio Institucional Eprints Complutense are freely accessible and property of the authors.

Prognosis The prognosis is variable and depends on the severity of the disease and any associated complications.

There was a problem providing the content you requested

Send link to edit together this prezi using Prezi Meeting learn more: De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria.

  AKASHIC RECORDS ATTUNEMENT PDF

Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare. Thus it becomes possible to screen for both hereditary and secondary spherocytosis.

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. Polish Academjy of Sciences?

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

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.

Este hecho explica la discrepancia entre estos valores. Este hecho explica la discrepancia entre estos valores. Monitoring of blood glucose and ferritin is recommended. Send the link below via email or IM Copy. Exchange transfusion diagnosstico performed in 3 children 1 with the severe form and 2 with the typical form of the disease.

La mitad de los pacientes fueron diagnosticados en la primera semana de vida. The identity of hyperchromic Diagnowtico and spherocytes as well as their normal percentage have been previously established. Se recomienda el monitoreo de glucemia y ferritina. HI estudio de un caso de Esferocitosis Familiar. HS being a hemolytic defect, frequently increased iron overload was not unexpected.