Robin N H, Abbadi N, McCandless S E, Nadeau J H
Center for Human Genetics, Case Western Reserve University School of Medicine and University Hospitals of Cleveland, Ohio 44106-6506, USA.
Am J Med Genet. 1997 Dec 31;73(4):425-36. doi: 10.1002/(sici)1096-8628(19971231)73:4<425::aid-ajmg11>3.0.co;2-t.
Disorganization (Ds) is a mouse mutant best known for producing an exceptional variety of unusual developmental anomalies, such as mirror-limb duplications and hamartomatous skin papillae. So great is the range of malformations that no two affected mice are identical. Several patients with a similar variety of exceptional anomalies have been reported, raising the possibility of the existence of a human homologue of Ds. However, although these human cases represent the most striking findings seen in Ds mice, they do not represent the full range of defects. Most affected mice have only a single malformation, and most of these malformations are similar to both common (neural tube defects, orofacial clefting, gastroschisis, limb reductions) and rare (anophthalmia, duplicated rectum) human birth defects. It is therefore possible that the full spectrum of the human homologue of Ds includes not only patients with the unusual combination of anomalies but also common sporadic birth defects. We suggest that the low penetrance (approximately 0-30%) and highly variable expression of Ds make it a paradigm for understanding the genetic basis for many seemingly sporadic birth defects.
紊乱(Ds)是一种小鼠突变体,以产生异常多样的发育异常而闻名,如镜像肢体重复和错构瘤性皮肤乳头。畸形范围如此之大,以至于没有两只受影响的小鼠是相同的。已经报道了几名有类似异常多样情况的患者,这增加了存在Ds人类同源物的可能性。然而,尽管这些人类病例代表了在Ds小鼠中看到的最显著的发现,但它们并不代表全部缺陷。大多数受影响的小鼠只有一种畸形,而且这些畸形大多数与常见的(神经管缺陷、口腔面部裂、腹裂、肢体短小)和罕见的(无眼、直肠重复)人类出生缺陷相似。因此,Ds人类同源物的全部范围可能不仅包括具有异常组合畸形的患者,还包括常见的散发性出生缺陷。我们认为,Ds的低外显率(约0 - 30%)和高度可变的表达使其成为理解许多看似散发性出生缺陷遗传基础的范例。