Skeletal Muscle Channelopathies.
Neurol Clin
; 38(3): 481-491, 2020 08.
Article
en En
| MEDLINE
| ID: mdl-32703462
ABSTRACT
Skeletal muscle channelopathies are rare genetic neuromuscular conditions that include the nondystrophic myotonias and periodic paralyses. They cause disabling muscle symptoms and can limit educational potential, work opportunities, socialization, and quality of life. Effective therapy is available, making it essential to recognize and treat this group of disorders. Here, the authors highlight important aspects regarding diagnosis and management using illustrative case reports.
Palabras clave
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Parálisis Periódica Hipopotasémica
/
Síndrome de Andersen
/
Canalopatías
Tipo de estudio:
Diagnostic_studies
Aspecto:
Patient_preference
Límite:
Adolescent
/
Humans
/
Male
Idioma:
En
Revista:
Neurol Clin
Año:
2020
Tipo del documento:
Article
País de afiliación:
Reino Unido