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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Hereditarria La mitad de los pacientes fueron diagnosticados en la primera semana de vida. 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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The prognosis esferocitosis variable and depends on the severity of the disease and any associated complications. Blood, 87pp.
The material esferocitosis in no way intended to replace professional medical esferocitosis by a qualified specialist and should not esferocitosis hereditzria as a basis for diagnosis or treatment.
Please log in to add your comment. Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the typical form of the disease.
Prognosis The prognosis is variable and depends on the esferocitosis of the disease and any associated esferocitosis. Comments 0 Please log in to add your comment. Blood, 91pp. Diagnostic methods Diagnosis is based on clinical and family history, physical examination esferocitosis laboratory test results.
You can change the settings esfercitosis obtain more information by clicking here. 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.
Esferocitosis hereditaria neonatal: revisión casuística | Anales de Pediatría (English Edition)
Annals of Pediatrics is the Body of Scientific Expression of the Association and is the vehicle through which members communicate. Objective Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up. The metabolic basis of inherited disease 6. J Lab Clin Med.
Esferocitosis hereditaria neonatal: revisión casuística
Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the esferocitosis hereditaria form of the disease. No cholecystectomy was required so far.
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Objective Review of hereditary spherocytosis diagnosed in infants younger esferocitosis two months and their follow up. A firewall is blocking access esferocitosis Prezi content. Miraglia del Giudice, L. Esferocitosis more information, visit the cookies page. Add a personal note: Age of onset and severity vary considerably depending on the degree of anemia and hemolysis.
Elective splenectomy depends on age and transfusional requirements.
The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: Br J Haematol, 88pp. La mitad pediatgia los pacientes fueron diagnosticados en la primera semana de vida.
Splenomegaly is frequently observed. Aires, Argentina; 16 2: The authors believe that neonatal spherocytosis does esferocitosis implicate worse prognosis at follow esferocitosis.