Hiraki Yoko, Okamoto Nobuhiko, Ida Tomoko, Nakata Yusei, Kamada Masahiro, Kanemura Yonehiro, Yamasaki Mami, Fujita Hiroko, Nishimura Gen, Kato Mitsuhiro, Harada Naoki, Matsumoto Naomichi
Hiroshima Municipal Center for Child Health and Development, Hiroshima, Japan.
Am J Med Genet A. 2008 May 15;146A(10):1241-7. doi: 10.1002/ajmg.a.32275.
We describe two new cases of pure 1q terminal deletions. BAC FISH analysis precisely defined the size of deletions. The first is a girl with 10.3-Mb deletion showed typical features of 1q43 deletion as well as a simplified gyral pattern, which was rarely found in 1q43 deletion. The other boy also presented with most of 1q43 deletion features but several atypical symptoms were noted including hydrocephalus, adducted thumbs, and flexion restriction of proximal interphalangeal joints in left hand. A concomitant novel missense mutation in L1CAM was identified in addition to 11.5-Mb deletion. Reviewing all the cases of pure 1q terminal deletion in the literature suggests that it is a clinically recognizable syndrome.
我们描述了两例新的纯1q末端缺失病例。BAC FISH分析精确确定了缺失的大小。第一例是一名患有10.3 Mb缺失的女孩,表现出典型的1q43缺失特征以及简化的脑回模式,这在1q43缺失中很少见。另一名男孩也表现出大部分1q43缺失特征,但注意到有一些非典型症状,包括脑积水、拇指内收和左手近端指间关节屈曲受限。除了11.5 Mb缺失外,还发现了L1CAM基因的一个新的错义突变。回顾文献中所有纯1q末端缺失病例表明,这是一种临床上可识别的综合征。