Esferocitosis hereditaria: Revisión. Parte I. Historia, demografía, etiopatogenia y diagnóstico. / [Hereditary spherocytosis: Review. Part I. History, demographics, pathogenesis, and diagnosis].
Arch Argent Pediatr
; 113(1): 69-80, 2015 Jan.
Article
em Es
| BINACIS
| ID: bin-133781
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.
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Texto completo:
1
Coleções:
01-internacional
/
06-national
/
AR
Base de dados:
BINACIS
/
LILACS
Assunto principal:
Esferocitose Hereditária
Tipo de estudo:
Diagnostic_studies
/
Etiology_studies
/
Risk_factors_studies
Limite:
Humans
Idioma:
Es
Revista:
Arch Argent Pediatr
/
Arch. argent. pediatr
Assunto da revista:
PEDIATRIA
Ano de publicação:
2015
Tipo de documento:
Article
País de afiliação:
Argentina
País de publicação:
Argentina