Arias S, Mota M
J Genet Hum. 1978 Jun;26(2):103-31.
Two large pedigrees with Waardenburg syndrome type I (W--I), i.e. with dystopia canthorum and blepharophimosis, are described to show both the variable expressivity of dystopia canthorum, which may be confused with non-penetrance of this sign, and the possibility to firmly diagnosis it with the new biometric index W, which differentiates a dystopic from a non-dystopic or a non-apparent dystopic subject, the latter within a defined biometric range. A general discussion of the relative value of blepharophimosis and dystopia canthorum as diagnostic features in W--I is presented, to conclude on the greater value of dystopia canthorum, which can be identified with confidence in more than 96% of carriers. Empirical probabilities are given for dystopia canthorum and blepharophimosis in the general populations, based on data from the world literature, useful for all ethnic groups.
本文描述了两个患有I型瓦登伯革氏综合征(W-I)的大家族,即伴有内眦异位和睑裂狭小。旨在展示内眦异位的可变表达性,这种表达性可能会与该体征的非外显现象相混淆,同时展示通过新的生物统计学指标W进行确诊的可能性,该指标能够区分内眦异位者与非内眦异位者或非明显内眦异位者(后者处于特定的生物统计学范围内)。本文还对睑裂狭小和内眦异位作为W-I诊断特征的相对价值进行了一般性讨论,得出内眦异位具有更大价值的结论,在超过96%的携带者中能够可靠地识别出内眦异位。基于来自世界文献的数据,给出了一般人群中内眦异位和睑裂狭小的经验概率,这对所有种族群体都有用。