Floor E, De Jong R O, Fryns J P, Smulders C, Vles J S
Department of Child Neurology, University Hospital, Maastricht, The Netherlands.
Clin Genet. 1989 Oct;36(4):236-41. doi: 10.1111/j.1399-0004.1989.tb03196.x.
This report gives a description of a three-generation family in which spondylocostal dysostosis associated with previously unreported neurological complaints occurred in five family members, suggesting autosomal dominant inheritance. A review of the literature is presented and previously unreported neurological complaints, e.g. neurogenic claudicatio, are emphasized.
本报告描述了一个三代家族，其中五名家族成员出现了与先前未报告的神经症状相关的脊椎肋骨发育不良，提示为常染色体显性遗传。本文还对文献进行了综述，并强调了先前未报告的神经症状，如神经源性间歇性跛行。
