Corbett Mark A, Turner Samantha J, Gardner Alison, Silver Jeremy, Stankovich Jim, Leventer Richard J, Derry Christopher P, Carroll Renée, Ha Thuong, Scheffer Ingrid E, Bahlo Melanie, Jackson Graeme D, Mackey David A, Berkovic Samuel F, Gecz Jozef
Adelaide Medical School, Robinson Research Institute, The University of Adelaide, Adelaide 5005, Australia.
Department of Paediatrics, The University of Melbourne Royal Children's Hospital, Parkville 3010, Australia; Neuroscience of Speech Group, Clinical Sciences Theme, Murdoch Children's Research Institute, Parkville 3052, Australia.
Eur J Med Genet. 2017 Aug;60(8):437-443. doi: 10.1016/j.ejmg.2017.06.002. Epub 2017 Jun 8.
Knobloch syndrome [OMIM: (KNO1) #267750] is a rare and clinically heterogeneous autosomal recessive disorder caused by mutations in COL18A1. Knobloch syndrome is characterised by abnormalities of the eye and occipital skull defects however the full phenotypic spectrum is yet to be defined. This report describes a family of four affected sisters with polymicrogyria, refractory seizures, and intellectual impairment of varying severity with a Lennox-Gastaut phenotype, and complex eye abnormalities where a syndromic diagnosis was not initially made. Whole exome sequencing of two affected sisters followed by filtering for rare and potentially disease causing variants in all genes identified compound heterozygous variants in NM_030582.3 (COL18A1): c.3690G > A: p.(Trp1230*) and NM_030582.3 (COL18A1): c.4063_4064delCT: p.(Leu1355Valfs*72). The two variants co-segregated with the affected individuals in the family. Identification of COL18A1 mutations in individuals with a Lennox-Gastaut phenotype and anterior polymicrogyria but lacking the classical occipital encephalocele expands the COL18A1 clinical spectrum.
诺布罗赫综合征[OMIM:(KNO1)#267750]是一种罕见的、临床异质性的常染色体隐性疾病,由COL18A1基因突变引起。诺布罗赫综合征的特征是眼部异常和枕骨颅骨缺损,然而其完整的表型谱尚未明确。本报告描述了一个四口之家,家中四姐妹均患病,她们患有多小脑回、难治性癫痫以及不同严重程度的智力障碍,具有伦诺克斯-加斯东综合征表型,还有复杂的眼部异常,最初未做出综合征诊断。对两名患病姐妹进行全外显子组测序,然后筛选所有基因中罕见的、可能致病的变异,在NM_030582.3(COL18A1)中鉴定出复合杂合变异:c.3690G>A:p.(Trp1230*)和NM_030582.3(COL18A1):c.4063_4064delCT:p.(Leu1355Valfs*72)。这两个变异在该家族中与患病个体共分离。在具有伦诺克斯-加斯东综合征表型和前部多小脑回但缺乏典型枕部脑膨出的个体中鉴定出COL18A1突变,扩大了COL18A1的临床谱。