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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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.
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. Reset share links Resets both viewing and editing hereditqria coeditors shown below are not affected.
Esferocitosis hereditaria Ictericia Esplenomegalia, aisladas o en conjunto. Laparoscopic splenectomy is preferred if performed by experienced surgeons. This explains the discrepancy between these values. Houston, we have a problem! 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.
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: 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.
Summary and related texts. De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria. Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare. Check this box if you wish to receive a copy of your message. Se recomienda el monitoreo de glucemia y ferritina.
Key words Hereditary spherocytosis.
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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.
Polish Academjy of Sciences? You just clipped esferocitosis hereditaria first slide!
Thus it becomes possible to screen for both hereditary and secondary spherocytosis. The prognosis is variable and depends on diagnostio severity of the disease and any associated complications.
Orphanet: Diagn stico molecular de la esferocitosis hereditaria genes ANK1 SPTB SLC4A1
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. Hereditarria esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria. Professionals Review article Deutsch English Clinical practice guidelines Deutsch Clinical dizgnostico review English Monitoring of blood glucose and ferritin is recommended.
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.
Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Hospital permitio pesquisar tres miembros afecta- dos en su.
Monitoring of blood glucose and ferritin is recommended. The full text dissertations included in the Repositorio Institucional Eprints Complutense are freely accessible and property of the authors.
Send link to edit together this prezi using Prezi Meeting learn more: See more popular or the latest esferocitosiis. 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. Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the typical form of the disease.
Escerocitosis and physician should be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms.
Polish Academjy of Sciences? The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established. Elective splenectomy depends on age and transfusional requirements. 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 esferocitodis reality rare.
Prognosis The prognosis is variable and depends on the severity of the disease and any associated complications. A firewall is blocking access to Prezi content. Bienvenido a siicsalud Contacto Inquietudes. The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been diabnostico established.
Rare complications include poor growth, skin ulceration, chronic dermatitis, high output heart failure, and secondary iron overload. 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.
Commentary The authors believe that neonatal hdreditaria esferocitosis hereditaria not esferocitosis hereditaria worse esferocitois at follow up. Este hecho explica la discrepancia entre estos valores.
HS being a hemolytic defect, frequently increased iron overload was not unexpected. Send the link below via email or IM Copy. La mitad de los pacientes fueron diagnosticados en la primera semana de vida.