Martínez-Frías M L, Bermejo Sánchez E, Arroyo Carrera I, Pérez Fernández J L, Pardo Romero M, Burón Martínez E, Hernández Ramón F
ECEMC, Facultad de Medicina, Universidad Complutense, Madrid.
An Esp Pediatr. 1999 Jan;50(1):57-60.
Townes-Brocks syndrome is constituted by a multi-systemic pattern of congenital anomalies with autosomal dominant inheritance. The most characteristic defects are those affecting hearing and the auricle, anal atresia and thumb anomalies.
We present the epidemiological characteristics of six cases of Townes-Brocks syndrome identified in the consecutive series of 25,967 malformed live born infants detected among 1,431,368 live births surveyed by the ECEMC (Spanish Collaborative Study of Congenital Malformations) between April 1976 and June 1997.
The minimal estimated frequency of Townes-Brocks syndrome in our data is 0.42 cases per 100,000 liveborn infants. These infants have low birth weights. Similar to other published studies, we have observed in our cases a wide variation in the clinical expression of the syndrome, showing great inter-family, as well as intrafamily variability.
汤姆斯-布罗克斯综合征由具有常染色体显性遗传的多系统先天性异常模式构成。最具特征性的缺陷是影响听力和耳廓、肛门闭锁及拇指异常。
我们呈现了在1976年4月至1997年6月期间由ECEMC(西班牙先天性畸形协作研究)调查的1,431,368例活产中检测出的25,967例畸形活产婴儿的连续系列中确诊的6例汤姆斯-布罗克斯综合征患者的流行病学特征。
我们数据中汤姆斯-布罗克斯综合征的最低估计发病率为每100,000例活产婴儿中有0.42例。这些婴儿出生体重低。与其他已发表的研究相似,我们在病例中观察到该综合征临床表现的广泛差异,显示出极大的家庭间以及家庭内变异性。