Lo L J, Noordhoff M S, Huang C S, Chen K T, Chen Y R
Department of Plastic and Reconstructive Surgery, Chang Gung Memorial Hospital, Taipei, Taiwan, R.O.C.
Cleft Palate Craniofac J. 1993 Nov;30(6):586-9. doi: 10.1597/1545-1569_1993_030_0586_pdotla_2.3.co_2.
A patient with bilateral complete cleft of the lip and palate (CLP) had a proximal deletion of the long arm of chromosome 1 (1q). This rare chromosomal abnormality was characterized by pre- and postnatal growth retardation, psychomotor retardation, and specific craniofacial and other systemic anomalies. There is a high incidence of CLP in proximal 1q deletion syndrome, especially bilateral CLP. Twelve other cases reported in the literature having this deletion and associated anomalies were reviewed.
一名双侧唇腭裂(CLP)患者发生了1号染色体长臂近端缺失(1q)。这种罕见的染色体异常表现为出生前和出生后的生长发育迟缓、精神运动发育迟缓以及特定的颅面和其他全身异常。在近端1q缺失综合征中,CLP的发病率很高,尤其是双侧CLP。对文献中报道的另外12例具有这种缺失及相关异常的病例进行了回顾。