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Cytogenet Genome Res ; 162(1-2): 40-45, 2022.
Artículo en Inglés | MEDLINE | ID: covidwho-1938106

RESUMEN

The 16p11.2 duplication is a well-known cause of developmental delay and autism, but there are only 2 previously reported cases of 16p11.2 triplication. Both of the previously reported cases exhibited tandem triplication on a 16p11.2 duplication inherited from 1 parent. We report fraternal twins presenting with developmental delay and 16p11.2 triplication resulting from inheritance of a 16p11.2 duplicated homolog from each parent. This report also reviews the overlapping features in previously published cases of 16p11.2 triplication, and possible implications are discussed.


Asunto(s)
Trastorno Autístico , Trastorno Autístico/genética , Duplicación Cromosómica/genética , Cromosomas Humanos Par 16/genética , Bases de Datos Genéticas , Femenino , Humanos , Masculino , Padres , Fenotipo
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