Gieron M A, Korthals J K, Kousseff B G
Am J Med Genet. 1985 Sep;22(1):143-7. doi: 10.1002/ajmg.1320220116.
We report on a mother and her three children with facioscapulohumeral dystrophy (FSHD), sensorineural hearing loss, and marked tortuosity of the retinal vessels. Initially the children presented with speech difficulties and hearing deficit. Hearing loss ranged from mild to severe. An audiologic evaluation, including brain stem auditory evoked responses in all patients, indicated a cochlear origin of hearing loss and intact pathways from the cochlea to the temporal lobe. The association of FSHD with hearing loss and tortuosity of the retinal vessels suggests previously unrecognized pleiotropy of FSHD (McKusick 15890) or a "new" type of FSHD.
我们报告了一位患有面肩肱型肌营养不良(FSHD)、感音神经性听力损失和视网膜血管显著迂曲的母亲及其三个孩子。最初,孩子们表现出言语困难和听力缺陷。听力损失程度从轻度到重度不等。所有患者均进行了包括脑干听觉诱发电位在内的听力学评估,结果表明听力损失起源于耳蜗,且从耳蜗到颞叶的传导通路完整。FSHD与听力损失及视网膜血管迂曲的关联提示了FSHD(麦库西克编号15890)之前未被认识到的多效性,或者是一种“新型”FSHD。