Dateki Sumito, Nakatomi Akiko, Watanabe Satoshi, Shimizu Hitomi, Inoue Yukiko, Baba Hideo, Yoshiura Koh-Ichiro, Moriuchi Hiroyuki
Department of Pediatrics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Department of Human Genetics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
J Hum Genet. 2017 Jul;62(7):717-721. doi: 10.1038/jhg.2017.33. Epub 2017 Mar 23.
Aggrecan is a critical proteoglycan component of the extracellular matrix of the growth plates and articular cartilage and has a key role in the biophysical and biomechanical properties of cartilage. Recently, heterozygous mutations in the ACAN gene, which encodes aggrecan, have been identified in patients with short stature and accelerated bone age. We herein report another family with a heterozygous ACAN mutation associated with idiopathic short stature along with accelerated bone age and early-onset herniation of the lumbar discs at the levels of L1/2 through L5/S1. Whole-exome sequencing identified a novel heterozygous frameshift mutation in the ACAN gene (c.1744delT; p.Phe582fs*69) in all of the affected family members but not in the unaffected one, providing further evidence that ACAN haploinsufficiency causes short stature with advanced bone maturation. In addition, we advocate early-onset multiple disc herniation as a novel phenotype associated with ACAN haploinsufficiency.
聚集蛋白聚糖是生长板和关节软骨细胞外基质的关键蛋白聚糖成分,在软骨的生物物理和生物力学特性中起关键作用。最近,在身材矮小和骨龄加速的患者中发现了编码聚集蛋白聚糖的ACAN基因突变。我们在此报告另一个家族,该家族存在与特发性身材矮小相关的杂合ACAN突变,同时伴有骨龄加速和L1/2至L5/S1水平的腰椎间盘早发性突出。全外显子测序在所有受影响的家庭成员中发现了ACAN基因中的一个新的杂合移码突变(c.1744delT;p.Phe582fs*69),而在未受影响的家庭成员中未发现,这进一步证明ACAN单倍体不足会导致身材矮小和骨成熟提前。此外,我们主张将早发性多发椎间盘突出作为与ACAN单倍体不足相关的一种新表型。