Oyama H, Kida Y, Tanaka T, Iwakoshi T, Niwa M, Kitamura R, Kobayashi T
Department of Neurosurgery, Komaki City Hospital, Aichi, Japan.
Neurol Med Chir (Tokyo). 1995 Jun;35(6):380-4. doi: 10.2176/nmc.35.380.
A 30-year-old male with Albright's hereditary osteodystrophy, pseudopseudohypoparathyroidism, and nephrogenic diabetes insipidus presented with hemifacial spasm persisting for 2 years. This association is extremely unusual. Angiography revealed markedly tortuous carotid and vertebral arteries inconsistent with his age. Neurovascular decompression of the left vertebral artery achieved only partial resolution of the spasm.
一名患有奥尔布赖特遗传性骨营养不良、假性假甲状旁腺功能减退和肾性尿崩症的30岁男性，出现半面痉挛持续2年。这种关联极为罕见。血管造影显示颈动脉和椎动脉明显迂曲，与他的年龄不符。对左椎动脉进行神经血管减压仅部分缓解了痉挛。
