C
Name Centronuclear Myopathies
Related to/Also known as Centronculear/Myotubular Myopathy;
Congenital Myopathies
Symptoms of Centronuclear Myopathy
Centronuclear and myotubular myopathy are rare inherited neuromuscular diseases of which there are three forms: x-linked, autosomal recessive, and autosomal dominant. The conditions manifest themselves as defects in the cell structure of voluntary muscles, causing low muscle tone and affecting children and adults at various stages in life.
Types  
Useful national contacts The Information Point for Centronuclear and Myotubular Myopathy
Email: This email address is being protected from spambots. You need JavaScript enabled to view it.
Link opens in new window http://centronuclear.org.uk
News and Events Survey: Treatment of Childhood Neurological Conditions (British Paediatric Neurology Association, September 2020)
Link opens in new window https://www.surveymonkey.co.uk/r/BPNA_JLA_RESEARCH_PSP
Online resources

Coronavirus - information for people with neurological problems (Brain & Spine Foundation)
Link opens in new window www.brainandspine.org.uk/coronavirus-covid-19

Myotubular/Centronuclear Myopathies (Contact, charity for families with dsabled children)
Link opens in new window https://tinyurl.com/v8x2rse

 Living with a condition (The Brain Charity)

Our resources The library at The Brain Charity has a range of resources on this condition and on a wide range of disability-related issues.