Arn P H, Mankinen C, Jabs E W
Nemours Children's Clinic, Jacksonville, Florida.
Am J Med Genet. 1993 Jun 15;46(5):534-6. doi: 10.1002/ajmg.1320460515.
We report on a patient with mild mandibulofacial dysostosis and a small interstitial deletion of 3p, 46,XY,del(3)(p23p24.12). Linkage of Treacher Collins syndrome, the most common of the mandibulofacial dysostoses, to the 5q31.3-->q33.3 region of chromosome 5 has been established. This is the fourth report of a patient with mandibulofacial dysostosis with a chromosome abnormality outside the 5q31.3 area. Mandibulofacial dysostosis is a heterogeneous entity, and evaluation and counseling of affected individuals should be undertaken with caution.
我们报告了一名患有轻度下颌面骨发育不全及3号染色体短臂小片段缺失(46,XY,del(3)(p23p24.12))的患者。最常见的下颌面骨发育不全——特雷彻·柯林斯综合征已被定位于5号染色体5q31.3→q33.3区域。这是第四例下颌面骨发育不全且染色体异常位于5q31.3区域之外的患者报告。下颌面骨发育不全是一种异质性疾病,对受累个体进行评估和咨询时应谨慎。