Lee Beom Hee, Cho Tae-Joon, Choi Hyun Jin, Kang Hee Kyung, Lim In Seok, Park Yong-Hoon, Ha Il Soo, Choi Yong, Cheong Hae Il
Department of Pediatrics, Seoul National University Children's Hospital, Seoul, Korea.
J Korean Med Sci. 2009 Jan;24 Suppl(Suppl 1):S82-6. doi: 10.3346/jkms.2009.24.S1.S82. Epub 2009 Jan 28.
Nail-patella syndrome (NPS) is an autosomal dominant disease that typically involves the nails, knees, elbows and the presence of iliac horns. In addition, some patients develop glomerulopathy or adult-onset glaucoma. NPS is caused by loss-of-function mutations in the LMX1B gene. In this study, phenotype-genotype correlation was analyzed in 9 unrelated Korean children with NPS and their affected family members. The probands included 5 boy and 4 girls who were confirmed to have NPS, as well as 6 of their affected parents. All of the patients (100%) had dysplastic nails, while 13 patients (86.7%) had patellar anomalies, 8 (53.3%) had iliac horns, 6 (40.0%) had elbow contracture, and 4 (26.7%) had nephropathy including one patient who developed end-stage renal disease at age 4.2. The genetic study revealed 8 different LMX1B mutations (5 missense mutations, 1 frame-shifting deletion and 2 abnormal splicing mutations), 6 of which were novel. Genotype-phenotype correlation was not identified, but inter- and intrafamilial phenotypic variability was observed. Overall, these findings are similar to the results of previously conducted studies, and the mechanism underlying the phenotypic variations and predisposing factors of the development and progression of nephropathy in NPS patients are still unknown.
指甲-髌骨综合征(NPS)是一种常染色体显性疾病,通常累及指甲、膝盖、肘部,并伴有髂骨角。此外,一些患者会出现肾小球病变或成人型青光眼。NPS由LMX1B基因功能丧失性突变引起。在本研究中,对9名无亲缘关系的韩国NPS患儿及其患病家庭成员进行了表型-基因型相关性分析。先证者包括5名男孩和4名女孩,他们均被确诊患有NPS,还有6名患病的父母。所有患者(100%)均有指甲发育异常,13例患者(86.7%)有髌骨异常,8例(53.3%)有髂骨角,6例(40.0%)有肘部挛缩,4例(26.7%)有肾病,其中1例患者在4.2岁时发展为终末期肾病。基因研究发现了8种不同的LMX1B突变(5种错义突变、1种移码缺失和2种异常剪接突变),其中6种是新发现的。未发现基因型-表型相关性,但观察到家族间和家族内的表型变异性。总体而言,这些发现与先前研究结果相似,NPS患者表型变异的机制以及肾病发生和进展的易感因素仍不清楚。