Leigh disease is a rare inherited neurometabolic disorder that affects the central
nervous system. It is named after Archibald Denis Leigh, a British ...
4 days ago ... Genetics Home Reference, Your Guide to Understanding Genetic Conditions ...
Leigh syndrome is a severe neurological disorder that usually ...
A collection of disease information resources and questions answered by our
Genetic and Rare Diseases Information Specialists for Leigh syndrome.
Leigh syndrome is a rare genetic neurometabolic disorder. It is characterized by
the degeneration of the central nervous system (i.e., brain, spinal cord, and optic
Leigh's Disease (Leigh's Syndrome) is a genetic disorder. Symptoms of Leigh's
disease include vomiting, irritability, seizures, loss of appetite, and loss of ...
These individuals are often referred to as having maternally inherited Leigh
syndrome (MILS). They harbor very high proportions (above 95%) of the ...
Mar 20, 2013 ... Leigh syndrome is a rare genetic neurometabolic disorder. It is characterized by
the degeneration of the central nervous system (i.e., brain, ...
A number sign (#) is used with this entry because of extensive genetic
heterogeneity in Leigh syndrome. Mutations have been identified in both nuclear-
Feb 16, 2010 ... Leighs disease is a form of rare inherited neuro-metabolic disorder that affects a
persons central nervous system.
You are not a carrier of Leigh syndrome. Your genome does not contain any of
the 26 mutations in 14 genes, known to cause Leigh syndrome. This means you ...