A sporadic case of charcot-marie-tooth disease type 2 with left vocal fold palsy due to mitofusin 2 mutation

Abstract

A 33-year-old Japanese woman was referred for hoarseness. She had been diagnosed with Charcot-Marie- Tooth disease at age 3 and bilateral optic atrophy at age 15. Laryngoscopy revealed left vocal fold palsy. These findings suggested Charcot-Marie-Tooth disease type 2; the diagnosis was confirmed by a mitofusin 2 mutation analysis. Her symptoms remained stable for almost 10 years. Although vocal fold palsy and optic atrophy have been previously reported in patients with mitofusin 2 mutations, detailed clinical information and clinical course have never been documented. These data might contribute to the elucidation of the pathological conditions associated with mitofusin 2 mutations.