Autosomal dominant cerebellar ataxia, deafness, and narcolepsy with amenorrhea, subclinical optic atrophy, and electroencephalographic abnormality: A case report

• Kai-Chieh Chang,
• Yih-Chih Kuo,
• Hsueh-Wen Hsueh,
• Ni-Chung Lee,
• Chih-Chao Yang,
• Sung-Tsang Hsieh,
• Chi-Chao Chao

Affiliations

Kai-Chieh Chang

Department of Neurology, National Taiwan University Hospital Yunlin Branch, Yunlin, Taiwan

Yih-Chih Kuo

Department of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan

Hsueh-Wen Hsueh

Department of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan; Corresponding author at: Department of Neurology, National Taiwan University Hospital, No. 7 Chung-Shan South Road, Taipei 10002, Taiwan.

Ni-Chung Lee

Department of Pediatric and Medical Genetics, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan

Chih-Chao Yang

Department of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan

Sung-Tsang Hsieh

Department of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan

Chi-Chao Chao

Department of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan