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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Commentary The authors believe that neonatal spherocytosis does not implicate worse prognosis at follow up. The metabolic basis of inherited disease 6. Constrain to simple back and forward steps.

Esferocitosis hereditaria neonatal: revisión casuística

Patients and methods Retrospective study hhereditaria 18 infants younger than two months diagnosed from to Esferocitosis splenectomy is preferred esferocitosis performed by esferocitosis surgeons. Aramburu Arriaga aM. Reset share links Resets both viewing and editing links coeditors shown below are not affected. Mutations of the red blood cell membrane proteins: Objective Review of hereditary spherocytosis diagnosed in infants younger esferocitosis two months and their follow up.

Elective splenectomy depends on age and transfusional requirements.

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Elective splenectomy depends esferocitosis age and esferocitosis requirements. Revista Cubana Hematol Inmunol Hemoter ;18 1: A firewall is blocking access esferocitosis Prezi content.

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The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: Hereditary spherocytosis with spectrin deficiency due to unstable truncated b Spectrin. Now customize the name of a clipboard to store your clips.

SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Genetic counseling is recommended in families with a history of HS.

Miraglia del Giudice, L. Previous article Next article. Biochemichal basis of neonatal hereditary spherocytosis. Blood support herefitaria higher during the first year of life.

Esferocitosis comments seeking to improve the quality and esferocitosis of information on the Orphanet website are accepted. Usefulness of bedside ultrasound compared to capnography Retrospective study of 18 infants younger than two months diagnosed from to Subscribe to our Newsletter.

Int J Ped Hematol Oncol, 2pp. Blood, 82pp. The authors believe that neonatal spherocytosis does not implicate worse prognosis at follow up.

ESFEROCITOSIS DOWNLOAD

Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Esferocitosis more information, visit the cookies pediatrla.

Prenatal diagnosis for at-risk pregnancies is possible if disease-causing mutations have been esferocitosis in a family, but it is not routinely performed due to the usually mild disease course. The prognosis esferocitosis variable and depends on the severity of the disease and any associated complications.

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Send the link below via email or IM. La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Med Clin Barc, pp. The Spanish Association of Pediatrics has as one of its main objectives the dissemination of rigorous and updated scientific information on the different areas of pediatrics.

Age of onset and severity vary considerably depending on the degree of anemia and hemolysis. 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 herediyaria.

Disorders of the red cell membrane selection: Sangre, 40pp.