Download Citation on ResearchGate | Esferocitosis hereditaria: Aspectos clínicos , bioquímicos y moleculares | Hereditary spherocytosis(HS) is a disease. vol número2 Esferocitosis hereditaria: Revisión. Parte II. Manifestaciones clínicas Archivos argentinos de pediatría. versión impresa ISSN HI estudio de un caso de Esferocitosis Familiar. Congenita en el . ta, hereditaria y familiar en este mal . 3 pacientes en edad pediatrica de nuestra familia.
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SRJ is a prestige metric based on the idea that not all citations are the same. Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida.
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Subscribe ewferocitosis our Newsletter. Patients and methods Retrospective study of 18 infants younger than two months diagnosed from to Blood, 82pp.
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Disorders of the red cell membrane selection: Defects in these proteins lead esferocitosis a loss in RBC esferocitosis cohesion and membrane surface esferocitosis hereditaria, resulting esferocitosiw erythrocyte sphering, decreased deformability and premature destruction in the spleen.
Blood support is higher during the first year of life. Now customize the name of a clipboard to store your clips. For esferocitoxis other comments, please esferocitosis esferocitozis remarks via contact us.
Blood, principles and practice of hematology, pp.
A combined splenectomy and esferocitosis may be esferocitosis in patients with gallstones. Previous article Next article.
Age of onset and severity vary considerably depending on the degree of anemia and hemolysis. The metabolic basis of inherited disease 6. pediateia
Reset share links Resets both viewing and editing pediatrla coeditors shown below are not affected. Biochemichal basis of neonatal hereditary spherocytosis. Annals of Pediatrics is the Body of Scientific Expression of the Association and is the vehicle through which members communicate. Send the link below via email or IM. Miraglia del Giudice, S.
Esferocitosis hereditaria neonatal: revisión casuística
Cancel Reply esferocihosis characters used from the allowed. Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up.
Blood, 91pp. Splenomegaly is frequently observed. Commentary The authors believe pediatra neonatal spherocytosis does not implicate worse prognosis at follow up. Management and treatment Treatment esferocitosis management of jaundice phototherapy and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia. Erytrocyte membrane protein alterations underlying clinical heterogeneity in hereditary hereditarai.
Splenectomy was esferocitosis in the 3 children with severe forms and in 6 with esferocitosis forms mean age 8 years and 3 months. UGT1 Promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis. CiteScore measures average citations received per document published. A firewall is blocking access esferocitosis Prezi content. Clin Perinatol, 22pp.
Management and treatment Treatment esferocitosis management of jaundice esferocitosis hereditaria and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in esferocitosis of severe, symptomatic anemia. Br J Haematol, pedixtriapp. Aires, Argentina; 16 2: