Fetal anomalies associated with an inversion duplication 13 chromosome.
Obstet Gynecol
; 71(6 Pt 2): 991-4, 1988 Jun.
Article
em En
| MEDLINE
| ID: mdl-3287254
ABSTRACT
We report the cytogenetics and pathology of a fetus with holoprosencephaly associated with an inversion duplication 13 chromosome. The pathology is compared with that found in cases of partial duplication (trisomy) and deficiency (monosomy) of chromosome 13 described in the literature. To our knowledge, this is the first time holoprosencephaly has been associated with this particular inversion duplication 13 chromosome. Careful pathology and complete chromosomal studies proved useful in counseling this couple.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Anormalidades Múltiplas
/
Cromossomos Humanos Par 13
/
Encéfalo
/
Aberrações Cromossômicas
/
Transtornos Cromossômicos
Tipo de estudo:
Diagnostic_studies
/
Risk_factors_studies
Limite:
Adult
/
Female
/
Humans
/
Pregnancy
Idioma:
En
Revista:
Obstet Gynecol
Ano de publicação:
1988
Tipo de documento:
Article