性幼稚——视网膜色素变性——多指(趾)畸形综合征,又称Lanrence-Moon-Biedl Sydrome,是一个罕见的先天性发育畸形,文献上很少有报道,现将我们见到的一例报告如下: 男性患儿,十一岁,维族,以自幼视物不清,肥胖,多指(趾)畸形于1977年10月6日入院。其父述患儿生后发现多指(趾),双眼发呆,视物不灵活,语言少,性情孤癖,食欲旺盛,食量大,体态渐肥胖。发育迟缓,于三岁时才会说话和 Sexual naïve - Retinitis pigmentosa - Multiple deformity syndrome, also known as Lanrence-Moon-Biedl Sydrome, is a rare congenital malformations, rarely reported in the literature, now we see an example Reported as follows: Male children, 11-year-old Uygur, as a child, blurred vision, obesity, multiple finger (toe) deformities in hospital on October 6, 1977. The father of children found after birth more fingers (toes), his eyes in a daze, blurred vision, less language, solitary addiction, appetite, food intake, the body gradually obese. Stunted, speaking at the age of three