Isik Esra, Onay Huseyin, Atik Tahir, Akgun Bilcag, Cogulu Ozgur, Ozkinay Ferda
Subdivision of Pediatric Genetics, Department of Pediatrics, Faculty of Medicine, Ege University, Izmir, Turkey.
Department of Medical Genetics, Faculty of Medicine, Ege University, Izmir, Turkey.
Clin Neurol Neurosurg. 2018 Sep;172:20-23. doi: 10.1016/j.clineuro.2018.06.007. Epub 2018 Jun 18.
L1 syndrome is a rare X linked recessive disorder caused bygene mutations in the L1 cell adhesion molecule (L1CAM), and characterized by hydrocephalus, intellectual disability, adducted thumbs and spasticity of the legs. The gene encodes a protein which plays an important role in neuronal development. Two unrelated L1 syndrome cases, with global developmental delay and hydrocephalus, were referred to pediatric genetics subdivision for genetic counseling. Bilateral adducted thumbs and spasticity in the lower extremities were also observed in both patients. Molecular analysis revealed two novel hemizygous mutations in the patients: a deletion mutation (c.749delG; p.Ser250Thrfs*51) and a splicing mutation (c.3166+1G>A). To conclude; in male patients with intellectual disability and hydrocephalus, where adducted thumbs are present, L1 syndrome should be considered.
L1综合征是一种罕见的X连锁隐性疾病,由L1细胞粘附分子(L1CAM)基因突变引起,其特征为脑积水、智力障碍、拇指内收和腿部痉挛。该基因编码一种在神经元发育中起重要作用的蛋白质。两名无亲缘关系的L1综合征病例,伴有全面发育迟缓及脑积水,被转诊至儿科遗传学部门进行遗传咨询。两名患者均观察到双侧拇指内收及下肢痉挛。分子分析显示患者存在两个新的半合子突变:一个缺失突变(c.749delG;p.Ser250Thrfs*51)和一个剪接突变(c.3166+1G>A)。总之,对于存在拇指内收的智力障碍和脑积水男性患者,应考虑L1综合征。