Osteogenesis imperfecta.
Curr Opin Pediatr
; 9(1): 94-9, 1997 Feb.
Article
em En
| MEDLINE
| ID: mdl-9088762
ABSTRACT
In the past 20 years, tremendous strides have been made in our understanding of the biochemical and genetic abnormalities associated with osteogenesis imperfecta (OI). Prenatal diagnostic techniques have allowed early detection of this disorder, particularly in families in which the actual molecular defect is already known. Although medical and surgical management of patients with OI continue to improve, the proper management of such problems as basilar impression still need to be determined. Progress in the treatment of OI at a molecular level is encouraging.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Osteogênese Imperfeita
Tipo de estudo:
Diagnostic_studies
/
Screening_studies
Limite:
Child
/
Humans
Idioma:
En
Revista:
Curr Opin Pediatr
Assunto da revista:
PEDIATRIA
Ano de publicação:
1997
Tipo de documento:
Article
País de afiliação:
Estados Unidos