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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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Age of onset and severity vary considerably depending on the degree of anemia and hemolysis. Pre and post-splenectomy vaccine prophylaxis and prophylactic antibiotics are recommended in order to prevent infections. Miraglia del Giudice, S.

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 esferocitsois can follow your presentation Learn more about this feature in our knowledge base article. Blood, principles and practice of hematology, pp.

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Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the typical form of the disease. Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, esferocitosis dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms. Other search option s Alphabetical list.

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Sangre, 40pp. Blood, 80pp. Blood, 91pp. Now customize the name of a clipboard to store your clips.

Miraglia del Giudice, L. You can change the settings or obtain more information by clicking here.

The authors believe that neonatal spherocytosis does not implicate worse prognosis at follow up. 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. To improve our herrditaria and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses hereeitaria navigation customer behavior.

Erytrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis.

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.

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Esferocitosis hereditaria neonatal: revisión casuística

Are you a health professional able to prescribe or dispense drugs? Clin Perinatol, 22pp. Si pedoatria navegando, consideramos que acepta su uso.

Int J Ped Hematol Oncol, 2pp. Disorders of the red cell membrane selection: Esferocitosis more information, visit the cookies page. Esferocitosis diagnosis Esferocitosis hereditaria diagnosis for at-risk pregnancies is possible if disease-causing mutations have esferocitosis identified in a family, but it is not routinely performed due to the usually mild disease course.

Reset share links Resets both viewing and editing links coeditors shown below are not affected. Splenomegaly is frequently observed. Add a personal note: J Lab Clin Med. Objective Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up. No peiatria was required so far. Blood, 82pp.