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Abstract:

Hereditary spherocytosis is the most frequent hereditary anemia excluding beta thalassemia in Argentina. Historical, demographic, genetic and pathogenic aspects of the disease are reviewed, and confirmatory laboratory tests are described. Special characteristics on the outcome of the disease in our population and prevalent protein deficiencies in our country are described. Emphasis is given on new available laboratory tests, which allow an earlier diagnosis using volume of blood samples significantly smaller than required for conventional tests.

Registro:

Documento: Artículo
Título:Hereditary spherocytosis. Review. Part I. History, demographics, pathogenesis, and diagnosis
Autor:Donato, H.; Crisp, R.L.; Rapetti, M.C.; García, E.; Attie, M.
Filiación:Sección Hematología/Oncología, Hospital del Niño de San Justo, Argentina
Consultorios de Hematología Infantil, Hospital del Niño de San Justo, Argentina
División Hematología Clínica, Hospital Nacional Prof. A. Posadas, Argentina
Departamento de Química Biológica, Facultad de Ciencias Exactas Y Naturales, Universidad de Buenos Aires, Argentina
División Hematología y Oncología Pediátrica, Hospital Nacional Prof. A. Posadas, Argentina
Servicio de Hematología, Hospital de Niños Ricardo Gutiérrez, Argentina
Palabras clave:Flow cytometry; Hemolytic anemia; Hereditary spherocytosis; Hyperbilirubinemia; Osmotic fragility; Article; blood sampling; demography; hereditary spherocytosis; heredity; human; laboratory test; medical history; outcome assessment; history; Spherocytosis, Hereditary; Demography; History, 19th Century; History, 20th Century; Humans; Spherocytosis, Hereditary
Año:2015
Volumen:113
Número:1
Página de inicio:69
Página de fin:80
DOI: http://dx.doi.org/10.5546/aap.2015.69
Título revista:Archivos Argentinos de Pediatria
Título revista abreviado:Arch. Argent. Pediatr.
ISSN:03250075
CODEN:AHAPA
Registro:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03250075_v113_n1_p69_Donato

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Citas:

---------- APA ----------
Donato, H., Crisp, R.L., Rapetti, M.C., García, E. & Attie, M. (2015) . Hereditary spherocytosis. Review. Part I. History, demographics, pathogenesis, and diagnosis . Archivos Argentinos de Pediatria, 113(1), 69-80.
http://dx.doi.org/10.5546/aap.2015.69
---------- CHICAGO ----------
Donato, H., Crisp, R.L., Rapetti, M.C., García, E., Attie, M. "Hereditary spherocytosis. Review. Part I. History, demographics, pathogenesis, and diagnosis " . Archivos Argentinos de Pediatria 113, no. 1 (2015) : 69-80.
http://dx.doi.org/10.5546/aap.2015.69
---------- MLA ----------
Donato, H., Crisp, R.L., Rapetti, M.C., García, E., Attie, M. "Hereditary spherocytosis. Review. Part I. History, demographics, pathogenesis, and diagnosis " . Archivos Argentinos de Pediatria, vol. 113, no. 1, 2015, pp. 69-80.
http://dx.doi.org/10.5546/aap.2015.69
---------- VANCOUVER ----------
Donato, H., Crisp, R.L., Rapetti, M.C., García, E., Attie, M. Hereditary spherocytosis. Review. Part I. History, demographics, pathogenesis, and diagnosis . Arch. Argent. Pediatr. 2015;113(1):69-80.
http://dx.doi.org/10.5546/aap.2015.69