Shirley Matthew D, Frelin Laurence, López José Soria, Jedlicka Anne, Dziedzic Amanda, Frank-Crawford Michelle A, Silverman Wayne, Hagopian Louis, Pevsner Jonathan
Program in Biochemistry, Cellular and Molecular Biology, Johns Hopkins School of Medicine, Baltimore, Maryland, United States of America.
Department of Neurology, Hugo W. Moser Research Institute at Kennedy Krieger, Baltimore, Maryland, United States of America.
PLoS One. 2016 Mar 2;11(3):e0149646. doi: 10.1371/journal.pone.0149646. eCollection 2016.
Copy number variants (CNVs) were detected and analyzed in 14 probands with autism and intellectual disability with self-injurious behavior (SIB) resulting in tissue damage. For each proband we obtained a clinical history and detailed behavioral descriptions. Genetic anomalies were observed in all probands, and likely clinical significance could be established in four cases. This included two cases having novel, de novo copy number variants and two cases having variants likely to have functional significance. These cases included segmental trisomy 14, segmental monosomy 21, and variants predicted to disrupt the function of ZEB2 (encoding a transcription factor) and HTR2C (encoding a serotonin receptor). Our results identify variants in regions previously implicated in intellectual disability and suggest candidate genes that could contribute to the etiology of SIB.
对14名患有自闭症、智力残疾且伴有自伤行为(SIB)导致组织损伤的先证者进行了拷贝数变异(CNV)检测与分析。对于每名先证者,我们获取了临床病史和详细的行为描述。在所有先证者中均观察到遗传异常,且在4例中确定了可能的临床意义。这包括2例具有新型、新发拷贝数变异的病例以及2例具有可能具有功能意义的变异的病例。这些病例包括14号染色体节段三体、21号染色体节段单体,以及预测会破坏ZEB2(编码一种转录因子)和HTR2C(编码一种血清素受体)功能的变异。我们的结果确定了先前与智力残疾相关区域的变异,并提出了可能导致自伤行为病因的候选基因。