Spinal and bulbar muscular atrophy is caused by polyglutamine expansion in the androgen receptor. As an X-linked disease dependent on androgens, symptoms and findings are only fully manifest in males. Here we describe a 40-year-old male-to-female transgender SBMA patient who developed full disease manifestations despite undetectable levels of androgens. We used cell culture and animal models to show that spironolactone, the anti-androgen she had taken for 15 years, promotes nuclear localization and toxicity of the mutant protein, which may explain the disease manifestations in this patient.
Sexual Reassignment Fails to Prevent Kennedy's Disease.
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作者:Lanman Tyler A, Bakar Dara, Badders Nisha M, Burke Ailbhe, Kokkinis Angela, Shrader Joseph A, Joe Galen O, Schindler Alice B, Bott Laura C, Harmison George G, Taylor J Paul, Fischbeck Kenneth H, Grunseich Christopher
| 期刊: | Journal of Neuromuscular Diseases | 影响因子: | 3.400 |
| 时间: | 2016 | 起止号: | 2016 Mar 3; 3(1):121-125 |
| doi: | 10.3233/JND-150128 | ||
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