Paramyotonia Congenita with Persistent Distal and Facial Muscle Weakness: A Case Report with Literature Review-Reference-Cited by-同舟云学术

Paramyotonia Congenita with Persistent Distal and Facial Muscle Weakness: A Case Report with Literature Review

Author:

Taminato Tomoya¹,Mori-Yoshimura Madoka¹,Miki Jun²,Sasaki Ryogen³,Sato Noriko⁴,Oya Yasushi¹,Nishino Ichizo⁵⁶,Takahashi Yuji¹

Affiliation:

1. Department of Neurology, National Center Hospital, National Center of Neurology and Psychiatry, Tokyo, Japan

2. Department of Neurology, Saku Central Hospital, Nagano Prefectural Federation of Agricultural Cooperatives for Health and Welfare, Nagano, Japan

3. Department of Neurology, Kuwana City Medical Center, Mie, Japan

4. Department of Radiology, National Center Hospital, National Center of Neurology and Psychiatry, Tokyo, Japan

5. Department of Genome Medicine Development, Medical Genome Center, National Center of Neurology and Psychiatry, Tokyo, Japan

6. Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan

Publisher

IOS Press

Subject

Clinical Neurology,Neurology

Reference62 articles.

1. Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus;Ptacek;Am J Hum Genet,1991

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2. Muscle channelopathies: A review;Annals of the Child Neurology Society;2023-10-10