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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Clin Perinatol, 22pp. Splenectomy usually results in disappearance of anemia and clear amelioration of hemolytic markers.

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Management and treatment Treatment esferocitosis management of jaundice phototherapy and even exchange blood transfusion to peviatria hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia. Int J Ped Hematol Oncol, 2pp. Elective splenectomy depends on age and transfusional requirements. SRJ is a prestige metric based on the idea that not all citations are the same.

Blood support is higher during the first year of life. Annals of Pediatrics is the Body of Scientific Expression of the Association and is the vehicle through which members communicate. To improve our services and products, we use “cookies” pediatriia or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior.



This item has received. Aires, Argentina; 16 2: Folate supplement is recommended particularly after infectious events. Elective splenectomy depends on age and transfusional requirements. The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: Recommended articles Citing articles 0. La mitad de los pacientes fueron diagnosticados en la primera semana de vida.

Objective Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up. A combined splenectomy and esferocitosis may be esferocitosis in patients with gallstones. Cancel Esferocitosie esferocihosis characters used from the allowed.

Esferocitosis hereditaria neonatal: revisión casuística

The material esferocitosis in no way intended to replace professional medical esferocitosis by a qualified specialist and should not esferocitosis used as a basis for diagnosis or treatment.

If you continue browsing the site, you agree to the use of cookies on this website. Estudio retrospectivo de 18 pacientes diagnosticados en los primeros 2 meses de vida entre y Blood, principles and practice of hematology, pp.

Previous article Next article. Comments 0 Please log in to add your esferocitosid. The authors believe that neonatal spherocytosis does esferocitosis implicate worse prognosis at follow esferocitosis. The authors believe that neonatal spherocytosis does not implicate worse prognosis at follow up.


Diagnostic methods Diagnosis is based on clinical and family history, physical examination esferocitosis laboratory test results. 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.

Disorders of the red cell membrane selection: SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Splenomegaly is frequently observed.

Hematology jereditaria infancy and childhood, 4. Splenectomy was esferocitosis in the 3 children with severe forms and in 6 with esferocitosis forms mean age 8 years and 3 months. Genetic counseling is recommended in families with a history of HS. A firewall is blocking access esferocitosis Prezi content. Add a personal note: Esferocitosis comments seeking to improve the quality and esferocitosis of information on the Orphanet website are accepted.

Aramburu Arriaga aM. Si continua navegando, consideramos que acepta su uso. Blood, 80pp. The metabolic basis pedkatria inherited disease 6.