Turnpenny P D, Thwaites R J, Boulos F N
Paediatric Department, The Nazareth Hospital, Israel.
J Med Genet. 1991 Jan;28(1):27-33. doi: 10.1136/jmg.28.1.27.
Seven members of a large inbred kindred with autosomal recessive spondylocostal dysostosis were examined clinically, radiographically, and sonographically. The subjects were three adults, one adolescent, and three children under 3 years of age. One child was the offspring of a first cousin marriage which showed quasi-dominant inheritance. Six subjects had short stature owing to widespread vertebral dyssegmentation with variable reduction in rib number and rib fusion. One subject was of normal stature, had limited vertebral dyssegmentation, an extra rib, and no rib fusion. Five subjects showed the plagiocephaly-torticollis sequence. Four of the five male subjects had inguinal herniation on one or both sides. All subjects had normal renal ultrasonography. The youngest subject died of cardiopulmonary complications and is thought to represent one extreme in the expressivity of the gene in this kindred.
对一个患有常染色体隐性脊柱肋骨发育不良的大型近亲家族的七名成员进行了临床、放射学和超声检查。受试者包括三名成年人、一名青少年和三名3岁以下儿童。一名儿童是近亲结婚的后代,表现出准显性遗传。六名受试者因广泛的椎体节段分化异常、肋骨数量不同程度减少和肋骨融合而身材矮小。一名受试者身材正常,椎体节段分化异常有限,有一根额外的肋骨,且无肋骨融合。五名受试者表现出头斜-斜颈序列征。五名男性受试者中有四名一侧或双侧患有腹股沟疝。所有受试者的肾脏超声检查均正常。最年幼的受试者死于心肺并发症,被认为代表了该家族中该基因表达的一个极端情况。