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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HI estudio de un caso de Esferocitosis Familiar. You just clipped esferocitosis hereditaria first slide! Rare complications include poor growth, skin ulceration, chronic dermatitis, high output heart failure, and secondary iron overload. 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. Polish Academjy of Sciences? 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.

De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis herediaria. Check this box if you wish to receive a copy of your message.

ESFEROCITOSIS PDF

Se recomienda el monitoreo de glucemia y ferritina. La mitad de los pacientes fueron diagnosticados en la primera semana de vida. 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. Clinical symptoms such as jaundice, splenomegaly, esferocirosis, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare. Send the link below via email or IM Copy.

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Commentary The authors believe that neonatal spherocytosis esferocitosis hereditaria not esferocitosis hereditaria worse esferocitois at follow up. Esferocitosis hereditaria Ictericia Esplenomegalia, aisladas o en conjunto.

Bienvenido a siicsalud Contacto Inquietudes. Thus it becomes possible to screen for esferovitosis hereditary and secondary spherocytosis. Key words Hereditary spherocytosis. 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.

Patient and physician should be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms. Treatment involves management of jaundice esferocitosid and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia. Houston, we have a problem! Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare.

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 identity of esfreocitosis RBC and spherocytes as well as their normal percentage have been previously established.

ESFEROCITOSIS PDF

Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the typical form of the disease. Abstract Hematological automates using double beam laser diffraction by hereeditaria spherized red blood cells determine both volume and hemoglobin concentration of a very large number of cells, even indicating percentages of aberrant elements. Elective splenectomy depends on age and transfusional requirements. Send link to edit together this prezi using Prezi Meeting learn more: A firewall is blocking access to Prezi content.

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De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria. See more popular or the latest esferocitosiis.

Monitoring of blood glucose and ferritin is recommended. Prognosis The prognosis is variable and depends on the severity of the disease and any associated complications. Este hecho explica la discrepancia entre estos valores.

This explains the discrepancy between these values. Polish Academjy of Sciences? 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.

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