Ruiter Mariken, Kamsteeg Erik-Jan, Meroni Germana, de Vries Bert B A
Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands Cluster in Biomedicine, Trieste, Italy.
Clin Dysmorphol. 2010 Oct;19(4):195-197. doi: 10.1097/MCD.0b013e32833dc5ee.
The X-linked Opitz G/BBB syndrome (OS) is a congenital malformation disorder characterized by hypertelorism, swallowing difficulties, hypospadias, and additional midline malformations. Loss of function mutations in the MID1 gene at Xp22.3 are responsible for the X-linked form of OS. Various mutations are found all over the gene but without a clear genotype-phenotype correlation. We describe additional family studies of a previously reported boy with a relatively mild form of OS, caused by the unique p.Lys370Glu (c.1108A>G) mutation in MID1. The same mutation was found in his clinically affected brother but also in the healthy maternal uncle. To our knowledge, this is the first report of a MID1 missense mutation causing non-penetrance in a male.
X连锁Opitz G/BBB综合征(OS)是一种先天性畸形疾病,其特征为眼距过宽、吞咽困难、尿道下裂以及其他中线畸形。位于Xp22.3的MID1基因功能丧失性突变导致了OS的X连锁形式。该基因各处均发现了各种突变,但基因型与表型之间没有明确的相关性。我们描述了对一名先前报道的患有相对轻度OS的男孩进行的额外家系研究,该男孩由MID1基因中独特的p.Lys370Glu(c.1108A>G)突变引起。在其临床受影响的兄弟中发现了相同的突变,在健康的舅舅中也发现了该突变。据我们所知,这是首次报道MID1错义突变在男性中导致非外显的情况。