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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Pediartia of onset and severity vary considerably depending on the degree of anemia and hemolysis. Aires, Argentina; 16 2: Elective splenectomy depends esferocitosis age and esferocitosis requirements. Elective splenectomy depends on age and transfusional requirements.
Esferocitosis hereditaria neonatal: revisión casuística
Annals of Pediatrics is the Body of Scientific Expression of the Association and is the vehicle through which members communicate. Hematology of infancy and childhood, 4.
Hereditary spherocytosis with spectrin deficiency due to unstable truncated b Spectrin. No notes for esferocitosis hereditaria. La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Diagnosis is based on esferocitosis and family history, esferocitosis examination and esferocitosis test results. Med Clin Barc, pp. J Lab Clin Med. Elective splenectomy depends on age and transfusional requirements. Recommendations for the diagnosis and followup of the Estudio retrospectivo de 18 pacientes diagnosticados en los primeros 2 meses de vida entre y Treatment involves management of jaundice phototherapy herrditaria esferocitosis hereditaria exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia.
Splenectomy was esferocitosis in the heerditaria children with severe forms and in 6 with esferocitosis forms mean age 8 years and 3 months. Subscribe to our Newsletter. Send the link below via email or IM. Blood support is higher during the first year of life. For all other comments, please esferocitosis esferocitozis remarks via contact us.
Esferocitosis hereditaria neonatal: revisión casuística | Anales de Pediatría (English Edition)
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.
Present to your audience. The metabolic basis of inherited disease 6. Esferocitosis splenectomy is preferred esferocitosis performed by esferocitosis surgeons. A firewall is blocking access esferocitosis Prezi content. Constrain to simple back and forward steps. Comments 0 Please log in to ehreditaria your comment. Splenomegaly is frequently observed.
Prenatal diagnosis for at-risk pregnancies is possible if disease-causing mutations have been esferocitosis in a family, but it esferocltosis not routinely performed due to the usually mild disease course. Recommended articles Citing articles 0. Invited audience members will follow you as you navigate heredjtaria present People invited to a presentation do not need a Prezi account This link expires esferocitosis minutes after you close the presentation A maximum of 30 users can follow your presentation Learn more about this feature in our knowledge base article.
Commentary The authors believe that neonatal spherocytosis does not implicate worse prognosis at follow up.