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Kennedy's disease

A clinicopathologic correlation with mutations in the androgen receptor gene

Departments of Neurology (Drs. Amato, Prior, and Mendell) and Pathology (Drs. Prior and Mendell, and P. Snyder and A. Papp), The Ohio State University, College of Medicine, Columbus, OH; and the Department of Neurology (Dr. Barohn), University of Texas Health Science Center, San Antonio, TX.

We confirmed a mutation of the androgen receptor gene as the cause for Kennedy's disease, also called "X-linked recessive spinal and bulbar muscular atrophy" or "bulbospinal neuronopathy." The mutation is characterized by an increased size of a polymorphic tandem CAG repeat within the first exon of the gene. The study population consisted of 17 patients from seven families (five distinct kinships and two isolated cases). Two patients were as yet asymptomatic and had normal examinations. Four carrier females showed the mutant as well as the normal allele; none showed clinical features of Kennedy's disease. There was no large expansion of the mutation observed in three generations of one family. Phenotypic expression between and within families was variable and not related to the size of the mutation. This contrasts with the gene mutations found in myotonic dystrophy and fragile X syndrome, where increased severity of disease correlates with the number of tandem triplet repeats. The findings reported here appear to explain the failure to find genetic anticipation in Kennedy's disease. The DNA test for Kennedy's disease can now be used for definitive diagnosis and carrier detection. In addition, mutation analysis allows early detection, which has implications for potential treatment.

Address correspondence and reprint requests to Dr. J.R. Mendell, Department of Neurology, Ohio State University, 1654 Upham Drive, Columbus, OH 43210

Received July 10, 1992. Accepted for publication in final form August 20, 1992

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