Autosomal Recessive Myotonia Congenita in an Adolescent Boy With Novel Mutation: A Case Report With Discussion on Management-Reference-Cited by-同舟云学术

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Autosomal Recessive Myotonia Congenita in an Adolescent Boy With Novel Mutation: A Case Report With Discussion on Management

Published:2024-02-10 Issue: Volume: Page:
ISSN:2168-8184
Container-title:Cureus
language:en
Short-container-title:

Author:

Das Palash,Panigrahi Debasis

Publisher

Springer Science and Business Media LLC

Reference8 articles.

1. Guidelines on clinical presentation and management of nondystrophic myotonias;Stunnenberg BC;Muscle Nerve,2020

2. The Clinical, Myopathological, and Genetic Analysis of 20 Patients With Non-dystrophic Myotonia;Wang Q;Front Neurol,2022

3. Myotonia congenita: novel mutations in CLCN1 gene;Liu XL;Channels (Austin),2015

4. Mexiletine in Myotonic Dystrophy Type 1: A Randomized, Double-Blind, Placebo-Controlled Trial;Heatwole C;Neurology,2021

5. Treatment Updates for Neuromuscular Channelopathies;Jitpimolmard N;Curr Treat Options Neurol,2020

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