Acetazolamide-responsive myotonia with a novel Ile239Thr mutation in
SCN4A gene
acetazolamide
case report
dive-bomber sound
sodium channel myotonia
Journal
Annals of medicine and surgery (2012)
ISSN: 2049-0801
Titre abrégé: Ann Med Surg (Lond)
Pays: England
ID NLM: 101616869
Informations de publication
Date de publication:
Feb 2024
Feb 2024
Historique:
received:
16
08
2023
accepted:
20
12
2023
medline:
9
2
2024
pubmed:
9
2
2024
entrez:
9
2
2024
Statut:
epublish
Résumé
Sodium channel myotonia (SCM) belongs to the group of sodium channelopathies with mutations involving The child presented with generalized muscle hypertrophy and stiffness involving arms, thighs, calves, chest, and back muscles with unusually prominent trapezius muscle. The parents described the warm-up phenomenon as an improvement in stiffness as the day passes and with repetitive action. Percussion myotonia was illustrated in the thenar eminence and trapezius muscle. Characteristic 'dive-bomber' sound was present in electromyography, and whole-exome sequencing revealed a novel Ile239Thr mutation in the This case presents a pure myotonic phenotype without episodes of weakness or paralysis. Generalized myotonia with muscle hypertrophy and demonstrating warm-up phenomenon resembles myotonia congenita (a chloride channelopathy). However, genetic analysis revealed a novel Ile239Thr mutation involving This case limelight sodium channel myotonia with a novel Ile239Thr mutation in
Identifiants
pubmed: 38333241
doi: 10.1097/MS9.0000000000001673
pii: AMSU-D-23-01757
pmc: PMC10849450
doi:
Types de publication
Case Reports
Langues
eng
Pagination
1191-1195Informations de copyright
Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc.
Déclaration de conflit d'intérêts
None.Sponsorships or competing interests that may be relevant to content are disclosed at the end of this article.