Nakai H, Adachi M, Katsushima N, Yamazaki N, Sakamoto M, Tada K
J Med Genet. 1983 Apr;20(2):142-4. doi: 10.1136/jmg.20.2.142.
A 2-year-old boy with mental and growth retardation is presented; he has a 46,XY,r(10)(p15q26) chromosome complement. Five previously reported cases of ring chromosome 10 were reviewed and compared with the present case in an attempt to delineate a clinical syndrome. Since the first description, identified by Giemsa banding by Lansky et al, four other r(10) patients have been described. Their common features were mental and growth retardation, low birth weight, microcephaly, stubby nose, hypertelorism, strabismus, wide set nipples, single transverse palmar creases, undescended testes, and hypoplastic scrotum. In some of the cases congenital heart disease was present.
报告了一名患有智力和生长发育迟缓的2岁男孩;其染色体核型为46,XY,r(10)(p15q26)。回顾了先前报道的5例环状10号染色体病例,并与本病例进行比较,试图勾勒出一种临床综合征。自Lansky等人通过吉姆萨染色首次描述以来,又描述了另外4例r(10)患者。他们的共同特征是智力和生长发育迟缓、低出生体重、小头畸形、短粗鼻、眼距过宽、斜视、乳头间距宽、单一横行掌褶、隐睾和阴囊发育不全。部分病例存在先天性心脏病。