Pierre-Robin sequence and severe mental retardation with chaotic behaviour associated with a small interstitial deletion in the long arm of chromosome 2 (del(2)(q331q333)).
Genet Couns
; 8(3): 249-52, 1997.
Article
em En
| MEDLINE
| ID: mdl-9327270
ABSTRACT
In this report we describe a severely mentally retarded male presenting an interstitial deletion in the long arm of chromosome 2 (del(2)(q331q333)). He presented a Pierre-Robin sequence at birth, and during childhood increasing behaviour problems were noted.
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Base de dados:
MEDLINE
Assunto principal:
Síndrome de Pierre Robin
/
Cromossomos Humanos Par 2
/
Transtornos do Comportamento Infantil
/
Deleção Cromossômica
/
Deficiência Intelectual
Tipo de estudo:
Risk_factors_studies
Limite:
Child
/
Humans
/
Male
Idioma:
En
Revista:
Genet Couns
Assunto da revista:
ETICA
/
GENETICA MEDICA
Ano de publicação:
1997
Tipo de documento:
Article
País de afiliação:
Bélgica