Kumar A, McCombs J L, Sapire D W
Department of Pediatrics, University of Texas Medical Branch 301, Galveston 77555-0367, USA.
Am J Cardiol. 1997 Feb 1;79(3):388-90. doi: 10.1016/s0002-9149(96)00772-2.
Two patients with cervical aortic arch are described, both with deletions in chromosome 22q11 region, and thymic hypofunction. This suggests that cervical aortic arch is part of the spectrum of the CATCH 22 group of defects.
描述了两名患有颈主动脉弓的患者，他们都存在22q11区域的染色体缺失以及胸腺功能减退。这表明颈主动脉弓是22q11微缺失综合征相关缺陷谱系的一部分。
