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Intern Med ; 58(14): 2091-2093, 2019 Jul 15.
Article in English | MEDLINE | ID: mdl-30996168

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.


Subject(s)
Charcot-Marie-Tooth Disease/complications , Charcot-Marie-Tooth Disease/genetics , GTP Phosphohydrolases/genetics , Mitochondrial Proteins/genetics , Optic Atrophy/genetics , Vocal Cord Paralysis/etiology , Vocal Cord Paralysis/genetics , Adolescent , Adult , Charcot-Marie-Tooth Disease/physiopathology , Child, Preschool , DNA Mutational Analysis , Female , Humans , Optic Atrophy/complications , Optic Atrophy/physiopathology , Vocal Cord Paralysis/physiopathology
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