Fryns J P, Vogels A, van den Berghe H
Center for Human Genetics, University of Leuven, Belgium.
Genet Couns. 1990;1(1):63-6.
A distinct entity?: In this report we describe the hitherto unreported association of low and middle frequency perceptive deafness and craniosynostosis in mother and son. The occurrence of hearing loss in the craniosynostosis syndromes is briefly reviewed.
一种独特的病症？：在本报告中，我们描述了此前未被报道的一对母子中低频感音神经性耳聋与颅缝早闭的关联。本文简要回顾了颅缝早闭综合征中听力损失的发生情况。
