Takeda Y, Itagaki M, Ishibashi K
Department of Oral Pathology, School of Dentistry, Iwate Medical University, Japan.
Int J Oral Maxillofac Surg. 1989 Apr;18(2):73-5. doi: 10.1016/s0901-5027(89)80132-8.
Hypoplastic-hypocalcified enamel of all permanent teeth and dysplasia of finger- and toe-nails were found in a 17-year-old Japanese male. Physical examination revealed no remarkable changes in skin, hair, sweat glands, bones, etc. Family history revealed the same abnormalities of teeth and nails in his mother's brother. A review of the literature concerning ectodermal dysplasia syndromes failed to reveal a combination of hypoplastic-hypocalcified enamel and dysplastic nails without changes in any other ectodermal tissues.
在一名17岁的日本男性中发现了所有恒牙的发育不全-钙化不全釉质以及指甲发育异常。体格检查显示皮肤、毛发、汗腺、骨骼等无明显变化。家族史显示他舅舅的牙齿和指甲也有同样的异常。对有关外胚层发育异常综合征的文献进行回顾后,未发现有发育不全-钙化不全釉质和指甲发育异常而其他外胚层组织无变化的组合情况。