Institut für Humangenetik, Universitätsklinikum Essen, Hufelandstr. 55, Essen 45122, Germany.
Hum Mutat. 2010 Jan;31(1):81-9. doi: 10.1002/humu.21142.
Werner mesomelic syndrome (WMS) is an autosomal dominant disorder with unknown molecular etiology characterized by hypo- or aplasia of the tibiae in addition to the preaxial polydactyly (PPD) of the hands and feet and/or five-fingered hand with absence of thumbs. We show that point mutations of a specific nucleotide within the sonic hedgehog (SHH) regulatory region (ZRS) cause WMS. In a previously unpublished WMS family, we identified the causative G>A transition at position 404 of the ZRS, and in six affected family members of a second WMS family we found a 404G>C mutation of the ZRS. The 404G>A ZRS mutation is known as the "Cuban mutation" of PPD type II (PPD2). Interestingly, the index patient of that family had tibial hypoplasia as well. These data provide the first evidence that WMS is caused by a specific ZRS mutation, which leads to strong ectopic SHH expression. In contrast, we show that complete duplications of the ZRS region lead to type Haas polysyndactyly or triphalangeal thumb-polysyndactyly syndrome, but do not affect lower limb development. We suggest the term "ZRS-associated syndromes" and a clinical subclassification for the continuum of limb malformations caused by different molecular alterations of the ZRS.
沃纳中胚层发育不良综合征(WMS)是一种常染色体显性遗传病,其分子病因不明,表现为手和脚的桡侧多趾(PPD)和/或五指畸形,伴或不伴有胫骨发育不良。我们发现 ZRS 内特定核苷酸的点突变导致 WMS。在一个未发表的 WMS 家系中,我们鉴定出 ZRS 第 404 位核苷酸的 G>A 转换,在第二个 WMS 家系的 6 位受累家系成员中发现 ZRS 的 404G>C 突变。该 404G>A ZRS 突变被称为 PPD Ⅱ型(PPD2)的“古巴突变”。有趣的是,该家系的先证者也存在胫骨发育不良。这些数据首次表明 WMS 是由特定的 ZRS 突变引起的,导致 SHH 异常表达。相比之下,我们发现 ZRS 区的完全重复会导致 Haas 型并指多趾畸形或三叉手并指多趾畸形综合征,但不会影响下肢发育。我们建议使用“ZRS 相关综合征”这一术语,并对由 ZRS 不同分子改变引起的肢体畸形连续谱进行临床亚分类。