Sorge G, Baieli S, Mauceri L, Greco F, Fiumara A
Department of Pediatric Neurology, Clinica Pediatrica dell'Università di Catania, Italy.
Am J Med Genet. 1998 Dec 4;80(4):403-5.
We studied a patient with microcephaly, short stature, type B brachydactyly, nail dysplasia, skeletal anomalies, and mental retardation. The mother of the propositus has brachydactyly of thumbs and a similar physiognomy without mental retardation. This appears to be another observation of the Tonoki syndrome, a distinct autosomal dominant or X-linked clinical entity.
我们研究了一名患有小头畸形、身材矮小、B型短指、指甲发育异常、骨骼异常和智力发育迟缓的患者。先证者的母亲有拇指短指和相似的相貌,但无智力发育迟缓。这似乎是对托诺基综合征的又一例观察,托诺基综合征是一种独特的常染色体显性或X连锁临床病症。