Discussion Topics: 0
Community Members: 1
Leigh Syndrome is a rare genetic disorder caused by mutations in mitochondrial DNA or by deficiencies of an enzyme called pyruvate dehydrogenase.
This community has no expert yet.
Leigh's Disease, Subacute Necrotizing Encephalomyelopathy, SNEM, X-Linked Leigh's Disease
Learn More About this Disorder
You have to join this community to be able to post messages on its forum or update its information.
It’s free and easy to join RareShare. Click here to signup for an account.
Gyrate Atrophy
about 9 hours ago
Hidradenitis Suppurativa
about 9 hours ago
Townes-Brocks Syndrome
about 10 hours ago
Syringomyelia
about 11 hours ago
Brown-Vialetto-Van Laere Syndrome
about 13 hours ago
Have questions about RareShare?
Visit our Frequently Asked Questions page to find the answers to some of the most commonly asked questions.