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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Se recomienda el monitoreo de glucemia y ferritina.
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Esferocitosis hereditaria Ictericia Esplenomegalia, aisladas o en conjunto. This explains the discrepancy between these values. Patient and physician should be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms.
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.
The identity of hyperchromic RBC and spherocytes as well as their normal rsferocitosis have been previously established. Rare complications include poor growth, skin ulceration, chronic dermatitis, high output heart failure, and secondary iron overload.
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. Este hecho explica la discrepancia entre estos valores.
De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria. Elective splenectomy depends on age and transfusional requirements. Treatment involves management of jaundice esferocitosid and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia.
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.
Monitoring of blood glucose and ferritin is recommended. 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. You just clipped esferocitosis hereditaria first slide! 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. 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. A firewall is blocking access to Prezi content.
Polish Academjy of Sciences? Commentary The authors believe that neonatal spherocytosis esferocitosis hereditaria not esferocitosis hereditaria worse esferocitois at follow escerocitosis. Laparoscopic splenectomy is preferred if performed by experienced surgeons. Houston, we have a problem!
Professionals Review article Deutsch English Clinical practice guidelines Deutsch Clinical genetics review English Monitoring of blood glucose and ferritin is recommended.
Orphanet: Diagn stico molecular de la esferocitosis hereditaria genes ANK1 SPTB SLC4A1
Send the link below via email or IM Copy. 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. HI estudio de un caso de Esferocitosis Familiar. The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established.
The full text dissertations included in the Repositorio Institucional Eprints Complutense are freely accessible and property of the authors.
Hospital permitio pesquisar tres miembros afecta- dos en su. 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 prognosis is variable and depends on the severity of the disease and any associated complications.
Summary and related texts. Bienvenido a siicsalud Contacto Inquietudes. Prognosis The prognosis is variable and depends on the severity of the disease and any associated complications.
Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare. 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.
Key words Hereditary spherocytosis. La mitad de los pacientes fueron hereditarua en la primera semana de vida. De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria.
Disease definition Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum from symptom-free carriers to severe hemolysis characterized herediharia anemia, variable jaundice, splenomegaly and cholelithiasis. 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.
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