Wells C R, Jankovic J
Arch Neurol. 1986 Sep;43(9):943-6. doi: 10.1001/archneur.1986.00520090071021.
We studied a large kindred with a chronic neurodegenerative disorder, affecting at least six male members in three generations. Spastic paraparesis, beginning at about 10 years of age, and hearing deficits were present in all affected members. Additionally, tremor ophthalmologic abnormalities, sensory deficits, short stature, hypogonadism, elevated cerebrospinal fluid protein, and absent or prolonged somatosensory evoked potentials were seen in some relatives. Although clinically similar to adrenomyeloneuropathy, the plasma and fibroblast levels of saturated very long-chain fatty acids were normal. This syndrome probably represents a new type of familial spastic paraparesis.
我们研究了一个患有慢性神经退行性疾病的大家族,该疾病在三代人中至少影响了六名男性成员。所有受影响成员均出现约10岁开始的痉挛性截瘫和听力缺陷。此外,一些亲属还出现了震颤、眼科异常、感觉缺陷、身材矮小、性腺功能减退、脑脊液蛋白升高以及体感诱发电位缺失或延长的情况。尽管在临床上与肾上腺脊髓神经病相似,但饱和极长链脂肪酸的血浆和成纤维细胞水平正常。这种综合征可能代表一种新型的家族性痉挛性截瘫。