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Familial Spastic Paraparesis and DeafnessA New X-linked Neurodegenerative Disorder
Christine R. Wells, MD;
Joseph Jankovic, MD
Arch Neurol. 1986;43(9):943-946.
Abstract
• 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.
Author Affiliations
From the Department of Neurology, Baylor College of Medicine, Houston.
Footnotes
Accepted for publication June 23, 1986.
Reprint requests to Department of Neurology, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030 (Dr Jankovic).
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