Becker congenital myotonia in black African with molecular findings

Becker congenital myotonia in black African with molecular findings

Abstract Background Congenital myotonia is a congenital disorder that affects skeletal muscles with myotonia. Affected muscles show stiffness and pain sometimes. The two major types of myotonia congenita are known as Thomsen disease and Becker disease. These conditions are distinguished by the sever...

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Bibliographic Details
Main Authors: Simon Azonbakin, Diane Adovoekpe, Marius Adjagba, Jules Alao, Gratien Sagbo, Constant Adjien, Anatole Laleye
Format: Article
Language:English
Published: SpringerOpen 2022-04-01
Series:Egyptian Journal of Medical Human Genetics
Subjects:
Myotonia
Congenital
Becker disease
CLCN1 gene
Mexiletine
Online Access:https://doi.org/10.1186/s43042-022-00290-0

Internet

https://doi.org/10.1186/s43042-022-00290-0

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