Name | Leigh Syndrome |
Related to/Also known as |
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Symptoms of Leigh Syndrome |
Leigh Syndrome is a rare, inherited, early-onset degenerative disorder with many different symptoms. This is a disease of the mitochondria, which provide energy for nerve cells in the brain and muscles. |
Types | X-linked Leigh Disease |
Useful national contacts | Metabolic Support UK (formerly known as Climb)![]() Tel. 0845 241 2173 The Leigh Network (Facebook) ![]() The Rare Mitochondrial Disease Service for Adults and Children (NHS) ![]() |
Children & young people |
INHERITED METABOLIC DISEASE AND CORONAVIRUS (COVID-19) Advice for patients / parents / guardians (Metabolic Support UK) NextGen (Metabolic Support (UK) Alex – Leigh’s Disease (Metabolic Support (UK) Leigh syndrome ('Contact' charity for families with disabled children) |
News and events | |
Online resources |
Guidance on shielding and protecting people defined on medical grounds as extremely vulnerable from COVID-19 (GOV.UK) Coronavirus Advice (Metabolic Support UK) Leigh Syndrome (Metabolic Support UK) Leigh Syndrome (U.S. National Organization for Rare Disorders) Leigh's Disease Information Page (U.S. National Institute for Neurological Disorders and Stroke) |
Our resources | The library at The Brain Charity has a range of resources on Leigh's Disease and on a wide range of disability-related issues. |