Volleth M, Erhardt J, Schmitzer E, Pfeiffer R A
Institut für Humangenetik, Friedrich-Alexander-Universität Erlangen-Nürnberg.
Monatsschr Kinderheilkd. 1993 Aug;141(8):655-8.
A 7 year old girl in whom an interstitial deletion of the short arm of a chromosome no. 4 had been discovered [46, XX, del(4)(p15.2p16)] is moderately retarded and exhibits some mild craniofacial dysmorphies. Cardiological examination revealed a PDA and an ASD. From seven similar cases published up to now a typical phenotype cannot be concluded. Dermatoglyphics show a remarkable frequency of digital arches but the diagnostic significance is questioned by this observation.
一名7岁女孩被发现存在4号染色体短臂的间质缺失[46, XX, del(4)(p15.2p16)],她中度智力发育迟缓,并有一些轻度的颅面畸形。心脏检查发现有动脉导管未闭和房间隔缺损。从目前已发表的7个类似病例中,无法得出典型的表型。皮纹学显示指纹弓出现频率显著,但这一观察结果对其诊断意义提出了质疑。