Christian J C, DeMyer Franken E A, Huff J S, Khairi S, Reed T
Clin Genet. 1977 Feb;11(2):128-36. doi: 10.1111/j.1399-0004.1977.tb01290.x.
A syndrome compatible with an X-linked trait is described, affecting four male cousins in three sibships. The body had skeletal anomalies, including short stature, ridging of the metopic suture, fusion of cervical vertebrae, thoracic hemivertebrae, scoliosis, sarcral hypoplasia and short middle phalanges. In addition, they had moderate developmental retardation, and abducens palsies. Three of the four had glucose intolerance, and one was born with an imperforate anus. Of five female obligate carriers studied, three had fusion of cervical vertebrae, three had some shortening of the middle phalanges and three had glucose intolerance. The syndrome in this family was compared to previously reported syndromes, and the conclusion was reached that it represents a previously unreported X-linked syndrome with minor manifestations in carrier females.
本文描述了一种与X连锁性状相符的综合征,该综合征影响了三个同胞家族中的四名男性表亲。这些患者身体存在骨骼异常,包括身材矮小、额缝隆起、颈椎融合、胸椎半椎体、脊柱侧凸、骶骨发育不全以及中指中节指骨短小。此外,他们还有中度发育迟缓及外展神经麻痹。四名患者中有三名存在葡萄糖耐受不良,一名出生时患有肛门闭锁。在研究的五名女性携带者中,三名有颈椎融合,三名有中指中节指骨轻度缩短,三名有葡萄糖耐受不良。将该家族中的综合征与先前报道的综合征进行比较后得出结论,它代表了一种先前未报道的X连锁综合征,在携带者女性中有轻微表现。