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Cytogenet Genome Res ; 146(2): 109-14, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26280689

RESUMO

Most apparent balanced chromosomal inversions are usually clinically asymptomatic; however, infertility, miscarriages, and mental retardation have been reported in inversion carriers. We present a small family with a paracentric inversion 1q42.13q43 detected in routine prenatal diagnosis. Molecular cytogenetic methods defined the size of the inversion as 11.7 Mb and excluded other unbalanced chromosomal alterations in the patients. Our findings suggest that intellectual disability is caused by dysfunction, disruption, or position effects of genes located at or near the breakpoints involved in this inversion.


Assuntos
Inversão Cromossômica , Cromossomos Humanos Par 1/genética , Doenças Fetais/genética , Deficiência Intelectual/genética , Diagnóstico Pré-Natal , Pré-Escolar , Bandeamento Cromossômico , Feminino , Doenças Fetais/diagnóstico , Humanos , Hibridização in Situ Fluorescente , Recém-Nascido , Deficiência Intelectual/diagnóstico , Gravidez
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