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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This item has received. Other search option s Alphabetical list. Int J Ped Hematol Oncol, 2pp.

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Blood support is higher during the first year of life. Med Clin Barc, pp.

No cholecystectomy was required so far. CiteScore measures average citations received per document published.

Are you a health professional able to prescribe or dispense drugs? Hematology basic principles pediartia practice, pp. Age of onset and severity vary considerably depending on the degree of anemia and hemolysis. A firewall is blocking access esferocitosis Prezi content.


Esferocitosis more information, visit the cookies page. The metabolic basis of inherited disease 6. Hematology of infancy and childhood, 4. Present to your audience Start remote presentation.


Splenectomy in the treatment of hemolytic anemia. Objective Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up. Annals of Pediatrics is the Body of Scientific Expression of the Association and is the vehicle through which members communicate. Mutations of the red blood cell pedaitria proteins: No notes for esferocitosis hereditaria. Send the link below via email or IM. Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida.

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. Elective splenectomy depends on age and transfusional requirements. SRJ is a prestige metric based on the idea that not all citations are the same.

Esferocitosis diagnosis Esferocitosis hereditaria diagnosis for at-risk pregnancies is possible if disease-causing mutations have esferocitosis identified herdditaria a family, but it is not routinely performed due to the usually mild disease course.

Miraglia del Giudice, S. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses pedkatria navigation customer behavior.


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. Now customize the name of a clipboard to store your clips. Diagnostic methods Hereditariq is based on clinical and family history, physical examination and laboratory test results.

Blood, 87pp. Four HS categories eeferocitosis been identified: UGT1 Promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis. The authors believe that neonatal spherocytosis does not implicate worse prognosis at follow up.

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.

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Splenectomy usually results in disappearance of anemia and clear amelioration of hemolytic markers. Miraglia del Giudice, L.