Cantwell R J
Humangenetik. 1975;26(3):261-5. doi: 10.1007/BF00281463.
A characteristic syndrome is described in which congenital sensori-neural deafness is associated not only with onychodystrophy but also with congenital bony anomalies the most characteristic of which are tri-phalangeal thumbs, bi-phalangeal digits of hands and feet, and dystrophic terminal phalanges of some of the fingers and toes. In addition, there is mental retardation and the dermatoglyphics are characterized by the presence of 10 arches and elevation of the atd angles. The syndrome is inherited as an autosomal recessive. It is suggested that this entity be named the D.O.O.R. Syndrome because of the deafness, onychodystrophy, osteodystrophy and retardation. A similar syndrome without retardation as described by Goodman et al. (1969) appears to be inherited as an autosomal dominant.
本文描述了一种特征性综合征,其中先天性感音神经性耳聋不仅与甲营养不良有关,还与先天性骨骼异常有关,其最典型的表现是拇指三节指骨、手足双节指骨以及部分手指和脚趾的末节指骨发育不良。此外,还存在智力发育迟缓,皮肤纹理学特征为有10个弓形纹且atd角增大。该综合征以常染色体隐性方式遗传。由于存在耳聋、甲营养不良、骨营养不良和发育迟缓,建议将这一病症命名为D.O.O.R.综合征。古德曼等人(1969年)描述的一种无发育迟缓的类似综合征似乎以常染色体显性方式遗传。