微缺失综合征
智力残疾
生物
自闭症
自闭症谱系障碍
遗传学
生物信息学
表型
医学
精神科
基因
作者
Julián Nevado,Rafaella Mergener,María Palomares,Karen Regina de Souza,Elena Vallespín,Rocío Mena,Víctor Martinez‐Glez,María Ángeles Mori,Fernando Santos,Sixto García‐Miñaúr,Fe Amalia García‐Santiago,Elena Mansilla,Luís Fernández,María Torres,Mariluce Riegel,Pablo Lapunzina
标识
DOI:10.1590/s1415-47572014000200007
摘要
Several new microdeletion and microduplication syndromes are emerging as disorders that have been proven to cause multisystem pathologies frequently associated with intellectual disability (ID), multiple congenital anomalies (MCA), autistic spectrum disorders (ASD) and other phenotypic findings. In this paper, we review the "new" and emergent microdeletion and microduplication syndromes that have been described and recognized in recent years with the aim of summarizing their main characteristics and chromosomal regions involved. We decided to group them by genomic region and within these groupings have classified them into those that include ID, MCA, ASD or other findings. This review does not intend to be exhaustive but is rather a quick guide to help pediatricians, clinical geneticists, cytogeneticists and/or molecular geneticists.
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