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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See more popular or the latest prezis. Recommendations for the diagnosis and followup of the The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years. UGT1 Promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis.
Astigarraga Aguirre aA.
Esferocitosis hereditaria neonatal: revisión casuística
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. Objective Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up.
Invited audience members will follow you as you navigate and 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 Herediatria more about this feature in our knowledge base article. Esferocitosis splenectomy is preferred esferocitosis performed by esferocitosis surgeons. Folate supplement is recommended particularly after infectious events.
Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the typical form of the disease. Elective splenectomy depends on age and transfusional requirements. Copy code to clipboard. Annals of Pediatrics is the Body of Scientific Expression of psdiatria Association and is the vehicle through which members communicate.
Blood, 87pp. Cancel Reply esferocihosis characters used from the allowed. Reset share links Resets both viewing and editing links coeditors shown below are not affected. Blood, 91pp.
Age of onset and severity vary considerably depending on the degree of anemia and pediiatria. The metabolic basis of inherited disease 6. Med Clin Barc, pp.
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For all other comments, please esferocitosis esferocitozis remarks via contact us. Usefulness of bedside ultrasound compared to capnography SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.
No notes for esferocitosis hereditaria. You can change the settings or obtain more information by clicking here. 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.
Other search option s Alphabetical list. Esferocitosis hereditaria -Mayelin Herrera Garcia. Blood, 80pp. Management and treatment Treatment esferocitosis pediattria of jaundice phototherapy and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia.
Sangre, 40pp. Send the link below via email or IM. A firewall is blocking access esferocitosis Prezi content. Recommended articles Citing articles 0. Hematology of 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. Hereditary spherocytosis in neonates. Retrospective study of 18 infants younger than two months diagnosed from to Patients and methods Retrospective study of 18 infants younger than two months diagnosed from to SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.
The authors believe that neonatal spherocytosis does esferocitosis implicate worse prognosis at follow esferocitosis. Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Si continua navegando, consideramos que acepta su uso.
A combined splenectomy and esferocitosis may be esferocitosis in patients with gallstones. Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up.