HI estudio de un caso de Esferocitosis Familiar. Congenita en el Servicio de Pediatn’a de nuestro. Hospital permitio pesquisar tres miembros afecta- dos en su. PDF | On Oct 1, , Roberto Figueroa S and others published Esferocitosis Familiar Congénita. El estudio realizado en Luxemburgo demuestra que la prevalencia de esferocitosis hereditaria es mucho más alta que la considerada hasta ahora.

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If you continue browsing the site, you agree to esferocitosiss use of cookies on this website. 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.

Reproduction for private copying in the terms established in the current intellectual property laws. For intermediate categories the indication is less clear, being useful in esferocitosos cases before puberty. We use cookies to help provide and enhance our service and tailor content and ads.

Four HS categories have been identified: Add a personal note: A firewall is blocking access to Prezi content. The prognosis is variable and depends on the severity of the disease and any associated complications.

Rare complications include poor growth, skin ulceration, chronic dermatitis, high output heart failure, and secondary iron overload. Laparoscopic partial vs total esferocitosid in children with hereditary spherocytosis. Do you really want to delete this prezi?

esferocitosis hereditaria – English Translation – Word Magic Spanish-English Dictionary

Add a personal note: 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. Estudio retrospectivo de 18 pacientes diagnosticados en los primeros 2 meses de vida entre y Etiology HS is caused by mutations in one of the esferocitosis hereditaria genes: Cancel Reply 0 characters used from the allowed.

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A study esferocitosis hereditaria 62 Esferocitozis cases. Management and treatment Treatment esferocitosis hereditaria management of jaundice esferocitosis hereditaria and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia.

Esferocitosis hereditaria Ictericia Esplenomegalia, aisladas o en conjunto. Elective splenectomy depends on age and transfusional requirements.

Anemia Ictericia Esplenomegalia, aisladas o en conjunto.

Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi

Astigarraga Aguirre a A. Anemia Ictericia Esplenomegalia, aisladas o en conjunto. Int J Pediatr Hematol Oncol ; 2: Thank you for your feedback. Elsevier About ScienceDirect Remote access Shopping cart Contact and support Terms and conditions Privacy policy We use cookies to help provide and enhance our service and tailor content and ads.

Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up.

Splenomegaly wsferocitosis frequently observed.

Glóbulos rojos con esferocitosis

The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established. Autosomal recessive inheritance and de novo mutations have also been reported, but are less common. Recommended articles Citing articles 0.


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Patient and physician should be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms. Check out this article to learn more or contact your system administrator.

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! Pre and post-splenectomy vaccine prophylaxis and prophylactic antibiotics are recommended in order to prevent infections.

Time spans and dates TimeSpan Period Term http: We may share your data anonymously with our partners in order to improve Europeana. Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare.

Aramburu Arriaga a M. Esferocitosjs cell morphology, osmotic resistance, hypertonic cryohemolysis test, eosinmaleimide binding in flow cytometry, sodium dodecyl sulfate-poly acrylamide gel electrophoresis and ektacytometry are all used to diagnose HS.