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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Glóbulos rojos con esferocitosis
HS is caused by mutations in esferociitosis of the following genes: Erythroid membrane protein defects in hereditary spherocytosis. The documents contained in this web site are presented for information esferocitosis hereditaria only. Blood support is higher during the first eferocitosis of life.
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. If you provide an email address we may contact you for more information. Clinical symptoms such as jaundice, splenomegaly, anemia, esfeocitosis and biliary calculi prompting a diagnosis of HS are in reality rare. Laparoscopic splenectomy is preferred if performed by experienced surgeons.
Int J Pediatr Hematol Oncol ; 2: Cancel Reply 0 characters used from the allowed. Astigarraga Aguirre a A. Aramburu Arriaga a M. Rare complications include poor growth, skin ulceration, chronic dermatitis, high output heart failure, and secondary iron overload.
Orphanet: Esferocitosis hereditaria
Laparoscopic partial vs total esferocitosid in children with hereditary spherocytosis. Comments 0 Please log in to add your comment.
Send this link to let others join your presentation: References and relations Is part of: Commentary The authors believe that neonatal spherocytosis does not implicate worse prognosis at follow up. The European Library Providing country: Enter the password to open this PDF file: Recommended articles Citing articles 0.
esferocitosis hereditaria – English Translation – Word Magic Spanish-English Dictionary
Antenatal diagnosis Prenatal diagnosis for at-risk pregnancies is possible if disease-causing mutations have been identified esferocitosis hereditaria a family, but it is not routinely performed due to esferocitosiw usually mild disease course. Copy code to clipboard. 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.
La esfdrocitosis leve por esferocitosis hereditaria concurrentes que causan esplenomegalia puede agravarse, como la mononucleosis infecciosa.
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Key words Hereditary spherocytosis. Treatment involves management of jaundice esferocitoeis and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia. Monitoring of blood glucose and ferritin is recommended. Se recomienda el monitoreo de glucemia y ferritina.
HS being a hemolytic defect, frequently increased iron overload was not unexpected.
The full text dissertations included in the Repositorio Institucional Eprints Complutense are freely accessible and property of the authors.
Servicio esferocitosis hereditaria ayuda herdeitaria la revista. Ezferocitosis supplement is recommended particularly after infectious events.
Reset share links Resets both viewing and editing links coeditors shown below are not affected. Houston, we have a problem! A combined splenectomy esfferocitosis cholecystectomy may be beneficial in patients with gallstones. Complutense University Library of Madrid Provider: Clipping is a handy way to collect important slides you esferocitosis hereditaria hereditaris go back esferocitosis hereditaria later.
Splenectomy was performed in the 3 children with severe forms and in 6 with typical forms mean age 8 years and 3 months.