Basel-Vanagaite L, Straussberg R, Friez M J, Inbar D, Korenreich L, Shohat M, Schwartz C E
Department of Medical Genetics, Rabin Medical Center, Beilinson Campus, Petah Tikva, Israel.
Clin Genet. 2006 May;69(5):414-9. doi: 10.1111/j.1399-0004.2006.00607.x.
Mutations in the L1CAM gene cause neurological abnormalities of variable severity, including congenital hydrocephalus, agenesis of the corpus callosum, spastic paraplegia, bilaterally adducted thumbs, aphasia, and mental retardation. Inter- and intrafamilial variability is a well-known feature of the L1CAM spectrum, and several patients have a combination of L1CAM mutations and Hirschsprung's disease (HSCR). We report on two siblings with a missense mutation in exon 7 (p.P240L) of the L1CAM gene. In one of the siblings, congenital dislocation of the radial heads and HSCR were present. Neither patient had hydrocephalus, adducted thumbs, or absent speech, but both had a hypoplastic corpus callosum. We suggest that L1CAM mutation testing should be considered in male patients with a positive family history compatible with X-linked inheritance and either the combination of agenesis of the CC and HSCR or the combination of agenesis of the CC and limb abnormalities, including abnormalities other than adducted thumbs.
L1CAM基因的突变会导致严重程度各异的神经学异常,包括先天性脑积水、胼胝体发育不全、痉挛性截瘫、双侧拇指内收、失语症和智力迟钝。家族间和家族内的变异性是L1CAM谱系的一个众所周知的特征,并且有几位患者同时存在L1CAM突变和先天性巨结肠症(HSCR)。我们报告了两名在L1CAM基因第7外显子存在错义突变(p.P240L)的兄弟姐妹。其中一名兄弟姐妹存在桡骨头先天性脱位和HSCR。两名患者均无脑积水、拇指内收或言语缺失,但均有胼胝体发育不全。我们建议,对于有与X连锁遗传相符的阳性家族史且存在胼胝体发育不全与HSCR的组合或胼胝体发育不全与肢体异常(包括除拇指内收以外的异常)的组合的男性患者,应考虑进行L1CAM突变检测。