Higurashi M, Oda M, Iijima K, Iijima S, Takeshita T, Watanabe N, Yoneyama K
Department of Maternal and Child Health, University of Tokyo, Japan.
Brain Dev. 1990;12(6):770-3. doi: 10.1016/s0387-7604(12)80004-0.
The results of a survey of the birth prevalence of congenital anomalies among 27,472 consecutive newborn babies at a large maternity hospital in Tokyo are reported. There were 29 cases with trisomy-21; 5 cases with trisomy-13 syndrome; 5 with trisomy-18 syndrome; 2 with cri-du-chat syndrome; and one each with partial monosomy 4p, partial trisomy 5p, partial trisomy 6p, partial trisomy 9p, partial trisomy 9q, partial monosomy 10p, and partial monosomy 13q. Single cases of the following were observed: the Hallermann-Streiff syndrome, the Treacher-Collins syndrome, achondroplasia, arthrogryposis, the Beckwith-Wiedemann syndrome, the asplenia syndrome, the Klippel-Trenaunay-Weber syndrome, the Marfan syndrome, the Carpenter syndrome, the Goldenhar syndrome, and the Pierre Robin syndrome. The results of follow-ups to determine the life-prognosis of each patient with an autosomal aberration are reported.
报告了对东京一家大型妇产医院连续27472名新生儿先天性异常出生患病率的调查结果。21三体综合征有29例;13三体综合征有5例;18三体综合征有5例;猫叫综合征有2例;4p部分单体、5p部分三体、6p部分三体、9p部分三体、9q部分三体、10p部分单体和13q部分单体各有1例。还观察到以下各1例:哈勒曼-施特雷夫综合征、特雷彻-柯林斯综合征、软骨发育不全、关节挛缩、贝-维综合征、无脾综合征、克-特-韦综合征、马方综合征、卡彭特综合征、戈尔登哈综合征和皮埃尔·罗宾综合征。报告了对每例常染色体畸变患者进行寿命预后评估的随访结果。