Babovic-Vuksanovic D, Jalal S M, Garrity J A, Robertson D M, Lindor N M
Department of Medical Genetics, Mayo Clinic, Rochester, Minnesota 55905, USA.
Am J Med Genet. 1998 Dec 4;80(4):373-6. doi: 10.1002/(sici)1096-8628(19981204)80:4<373::aid-ajmg13>3.0.co;2-m.
We describe a 20-year-old man with Smith-Magenis syndrome and a 46,XY,del(17)(p11.2p11.2) karyotype. The interstitial deletion was confirmed by metaphase analysis using the fluorescent in situ hybridization probe (D17S29) for the Smith-Magenis region. The patient had hypertelorism, exotropia, and high myopia. Examination under anesthesia showed a lacquer crack near the right macula and a disciform scar of the left macula. Six months later, the patient presented with subacute visual loss. Examination demonstrated end-stage macula degeneration with bilateral disciform scars. There was no evidence of retinal detachment. Prior reports of Smith-Magenis syndrome mention telecanthus, ptosis, strabismus, iris anomalies, cataract, microcornea, optic nerve hypoplasia, myopia, retinal detachment, and lattice retinal degeneration. Bilateral macular degeneration has not been reported previously, and it may be an additional ophthalmologic manifestation of Smith-Magenis syndrome, either as a primary manifestation or as a direct consequence of high myopia.
我们描述了一名患有史密斯-马吉尼斯综合征的20岁男性,其核型为46,XY,del(17)(p11.2p11.2)。通过使用针对史密斯-马吉尼斯区域的荧光原位杂交探针(D17S29)进行中期分析,证实了间质缺失。该患者有眼距过宽、外斜视和高度近视。麻醉下检查显示右黄斑附近有漆裂纹,左黄斑有盘状瘢痕。六个月后,患者出现亚急性视力丧失。检查显示终末期黄斑变性伴双侧盘状瘢痕。没有视网膜脱离的证据。先前关于史密斯-马吉尼斯综合征的报道提到了内眦距过宽、上睑下垂、斜视、虹膜异常、白内障、小角膜、视神经发育不全、近视、视网膜脱离和格子状视网膜变性。双侧黄斑变性以前尚未见报道,它可能是史密斯-马吉尼斯综合征的一种额外眼科表现,要么作为主要表现,要么作为高度近视的直接后果。