Chen A, Francis M, Ni L, Cremers C W, Kimberling W J, Sato Y, Phelps P D, Bellman S C, Wagner M J, Pembrey M
Department of Otolaryngology-Head and Neck Surgery, University of Iowa, Iowa City 52242, USA.
Am J Med Genet. 1995 Sep 25;58(4):365-70. doi: 10.1002/ajmg.1320580413.
Branchiootorenal (BOR) syndrome is a variable, autosomal-dominant disorder of the first and second embryonic branchial arches, kidneys, and urinary tract. We describe the phenotype in 45 individuals, highlighting differences and similarities reported in other studies. Characteristic temporal bone findings include cochlear hypoplasia (4/5 of normal size with only 2 turns), dilation of the vestibular aqueduct, bulbous internal auditory canals, deep posterior fossae, and acutely-angled promontories.
鳃耳肾(BOR)综合征是一种累及第一和第二胚胎鳃弓、肾脏及泌尿道的常染色体显性疾病,其表现多样。我们描述了45例患者的表型,强调了与其他研究报道的异同。颞骨的特征性表现包括耳蜗发育不全(大小为正常的4/5,仅2圈)、前庭导水管扩张、内耳道呈球茎状、后颅窝深以及岬角呈锐角。