Turleau C, de Grouchy J, Chavin-Colin F, Roubin M, Brissaud P E, Repessé G, Safar A, Borniche P
Humangenetik. 1975 Sep 23;29(3):233-41. doi: 10.1007/BF00297629.
Two unrelated patients with a strikingly similar phenotype (low birth weight and poor thriving; mental retardation; dolichocephaly; beaked nose; deeply set eyes; prominent maxilla and receding small chin; long fingers with a peculiar clench) were partially trisomic for two different segments of 9q. The segment found to be trisomic in both patients is small and corresponds to the q31q32 region. This new syndrome is compared to observations of trisomy 9 reported in the literature.
两名无血缘关系的患者具有极为相似的表型(低出生体重且生长发育不良;智力迟钝;长头畸形;鹰钩鼻;眼窝深陷;上颌突出且小下巴后缩;手指细长且握拳姿势奇特),均为9号染色体长臂两个不同片段的部分三体。在两名患者中均发现三体的片段很小,对应于q31q32区域。将这种新综合征与文献中报道的9号染色体三体的观察结果进行了比较。