Hartsfield J K, Hall B D, Grix A W, Kousseff B G, Salazar J F, Haufe S M
University of South Florida, College of Medicine, Department of Pediatrics, Tampa 33612-4799.
Am J Med Genet. 1993 Mar 1;45(5):552-7. doi: 10.1002/ajmg.1320450505.
We report on 7 patients (6 M, 1 F) with Coffin-Lowry syndrome who have a sensorineural hearing deficit in addition to developmental delay and characteristic facial changes. One of the patients also had a history of premature exfoliation of primary teeth. These are previously unappreciated clinical signs that may aid in the early diagnosis of Coffin-Lowry syndrome. Early diagnosis and recognition of a hearing deficit in the patient can lead to the use of hearing aids to help the patient achieve his or her full potential. These "new" clinical manifestations expand the phenotype of Coffin-Lowry syndrome and constitute an additional indication of pleiotropy.
我们报告了7例患有科芬-洛里综合征的患者(6名男性,1名女性),他们除了有发育迟缓及典型的面部特征外,还存在感音神经性听力缺陷。其中1例患者还有乳牙过早脱落的病史。这些都是以前未被认识到的临床体征,可能有助于科芬-洛里综合征的早期诊断。早期诊断并识别患者的听力缺陷可促使使用助听器,帮助患者充分发挥其潜能。这些“新的”临床表现扩展了科芬-洛里综合征的表型,构成了基因多效性的又一证据。