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Leigh disease

en.wikipedia.org/wiki/Leigh_disease

Leigh disease, also known as juvenile subacute necrotizing encephalomyelopathy, Leigh ... Different genetic causes and types of Leigh syndrome have different prognoses, though all are poor. The most...

Leigh syndrome - Genetics Home Reference

ghr.nlm.nih.gov/condition/leigh-syndrome

Leigh syndrome is a severe neurological disorder that typically arises in the first year of life. This condition is characterized by progressive loss of mental and ...

Leigh Syndrome - NORD (National Organization for Rare Disorders)

rarediseases.org/rare-diseases/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): Read About Treatments

www.medicinenet.com/leighs_syndrome_leighs_disease/article.htm

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 ...

Gentle Results | Leigh syndrome

results.gentlelabs.com/leigh-syndrome

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 ...

Leigh Syndrome - WebMD

www.webmd.com/children/leighs-disease

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 - Facts and Information - Disabled World

www.disabled-world.com/disability/types/leighs-disease.php

Feb 16, 2010 ... Leighs disease is a form of rare inherited neuro-metabolic disorder that affects a persons central nervous system.

OMIM Entry - # 256000 - LEIGH SYNDROME; LS

www.omim.org/entry/256000

A number sign (#) is used with this entry because of extensive genetic heterogeneity in Leigh syndrome. Mutations have been identified in both nuclear- and ...

Texas Boy Battles Rare Leigh's Disease - ABC News

abcnews.go.com/Health/Wellness/texas-boy-battles-rare-leighs-disease/story?id=17375005

Oct 3, 2012 ... Will has Leigh's disease, a genetic disorder that affects one in 40,000 newborns. And although his case is mild, he's unlikely to live past his ...

A rare mitochondrial disorder: Leigh syndrome - a case report ...

ijponline.biomedcentral.com/articles/10.1186/1824-7288-36-62

Leigh Syndrome [1], also termed as subacute necrotising encephalopathy is a rare, inherited progressive neurodegenerative disorder with characteristic ...

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Leigh's Disease Information Page: National Institute of Neurological ...

www.ninds.nih.gov

Dec 16, 2011 ... Leigh's disease is a rare inherited neurometabolic disorder that affects the central nervous system. This progressive disorder begins in infants ...

Leigh's Disease - The United Mitochondrial Disease Foundation

www.umdf.org

Leigh's Disease is a progressive neurometabolic disorder with a general onset ... II, IV, and V. Depending on the defect, the mode of inheritance may be X-linked ...

Orphanet: Leigh syndrome

www.orpha.net

Synonym(s), Infantile subacute necrotizing encephalopathy. Leigh disease. Prevalence, Unknown. Inheritance, Autosomal recessive or X-linked recessive