The 9p- deletion syndrome. A patient with a 45, XX-9, -15, +t(9/15) constitution due to maternal 3:1 meiotic disjunction.
Clin Genet
; 11(3): 219-23, 1977 Mar.
Article
em En
| MEDLINE
| ID: mdl-837573
ABSTRACT
Deletion of the short arm of chromosome 9, derived from a 31 meiotic segregation in the mother, carrier of a balanced 9/15 translocation, was found in a 3-year-old female. Severe psychomotor retardation with delayed speech, brachicephaly, flat occiput hypertelorism and long upper lip were the main signs in the girl.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Aberrações Cromossômicas
/
Deleção Cromossômica
/
Cromossomos Humanos 13-15
/
Cromossomos Humanos 6-12 e X
Limite:
Child, preschool
/
Female
/
Humans
Idioma:
En
Revista:
Clin Genet
Ano de publicação:
1977
Tipo de documento:
Article