Batten-Turner Congenital Myopathy

Alias:
Myotonia Congenita
Congenital Myotonia
Thomsen and Becker Disease
Congenital Myotonic Muscular Dystrophy
Batten Turner Congenital Myopathy
Generalized Myotonia of Thomsen
Myotonia Congenita Nos
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Batten-Turner Congenital Myopathy, also known as myotonia congenita, is related to myotonia and myotonic dystrophy, and has symptoms including muscular stiffness and lid lag. An important gene associated with Batten-Turner Congenital Myopathy is CLCN1 (Chloride Voltage-Gated Channel 1), and among its related pathways/superpathways are Activation of cAMP-Dependent PKA and Transport of inorganic cations/anions and amino acids/oligopeptides. The drugs Lamotrigine and Mexiletine have been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle and tongue, and related phenotypes are myotonia and emg abnormality
Related ID:
MESH:D009224
ICD11:1916703439

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
1-9/100000
19
170
57

Medical Symptom

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Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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No data available

Disease Model

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Name
MGI
Related Gene
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Publications
No data available

References Literature

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