Literature DB >> 18313341

Extraocular muscle hypertrophy in myotonia congenita.

Bradley Wakeman1, Deepti Babu, Jack Tarleton, Ian M Macdonald.   

Abstract

Myotonia congenita (MC) is a rare disorder of skeletal muscle caused by mutations in the CLCN1 gene,(1,2) which encodes the chloride ion channel found in the t-tubule of skeletal muscle. MC is characterized by impaired relaxation of voluntary muscle after sudden contraction that diminishes with muscle activity, known as the "warm-up effect." Individuals with MC can develop muscular hypertrophy despite little physical activity. Esotropia and reduced saccadic velocities have been reported in the dominant form of MC. We report two cases in which orbital magnetic resonance imaging (MRI) imaging showed extraocular muscle hypertrophy.

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Year:  2008        PMID: 18313341     DOI: 10.1016/j.jaapos.2007.12.002

Source DB:  PubMed          Journal:  J AAPOS        ISSN: 1091-8531            Impact factor:   1.220


  5 in total

Review 1.  Mutations of SCN4A gene cause different diseases: 2 case reports and literature review.

Authors:  Xiao-li Liu; Xiao-jun Huang; Xing-hua Luan; Hai-yan Zhou; Tian Wang; Jing-yi Wang; Sheng-di Chen; Hui-dong Tang; Li Cao
Journal:  Channels (Austin)       Date:  2015       Impact factor: 2.581

2.  Sodium Channel Myotonia and a Novel Gly701Asp Mutation in the SCN4A Gene: From an Ophthalmological Symptom to a Familial Disease.

Authors:  Filipa Sampaio; Sérgia Soares; Sara Pereira; José Alberto Lemos; Ágata Mota
Journal:  Neuroophthalmology       Date:  2020-07-24

3.  Myotonia congenita with strabismus in a large family with a mutation in the SCN4A gene.

Authors:  H Du; S R Grob; L Zhao; J Lee; M El-Sahn; G Hughes; J Luo; K Schaf; Y Duan; J Quach; X Wei; P Shaw; D Granet; K Zhang
Journal:  Eye (Lond)       Date:  2012-06-01       Impact factor: 3.775

4.  A de novo Mutation in the SCN4A Gene Causing Sodium Channel Myotonia.

Authors:  Kristin Ørstavik; Sean Ciaran Wallace; Torberg Torbergsen; Angela Abicht; Svein Erik Tangsrud; Emilia Kerty; Magnhild Rasmussen
Journal:  J Neuromuscul Dis       Date:  2015-06-04

5.  Imaging alterations in skeletal muscle channelopathies: a study in 15 patients.

Authors:  Lorenzo Maggi; Raffaella Brugnoni; Eleonora Canioni; Elio Maccagnano; Pia Bernasconi; Lucia Morandi
Journal:  Acta Myol       Date:  2015-12
  5 in total

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