Assessment
Questionnaire

Have a symptom?
See what questions
a doctor would ask.
 

Leber optic atrophy

Leber optic atrophy: Introduction

Leber optic atrophy: An inherited biochemical disorder due to mitochondrial mutation. More detailed information about the symptoms, causes, and treatments of Leber optic atrophy is available below.

Symptoms of Leber optic atrophy

Home Diagnostic Testing

Home medical testing related to Leber optic atrophy:

Wrongly Diagnosed with Leber optic atrophy?

Leber optic atrophy: Related Patient Stories

Leber optic atrophy: Complications

Read more about complications of Leber optic atrophy.

Causes of Leber optic atrophy

Read more about causes of Leber optic atrophy.

Disease Topics Related To Leber optic atrophy

Research the causes of these diseases that are similar to, or related to, Leber optic atrophy:

Leber optic atrophy: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Leber optic atrophy: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Evidence Based Medicine Research for Leber optic atrophy

Medical research articles related to Leber optic atrophy include:

Click here to find more evidence-based articles on the TRIP Database

Leber optic atrophy: Animations

Research about Leber optic atrophy

Visit our research pages for current research about Leber optic atrophy treatments.

Statistics for Leber optic atrophy

Leber optic atrophy: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Leber optic atrophy, or answer someone else's question, on our message boards:

Definitions of Leber optic atrophy:

A maternally linked genetic disorder that presents in mid-life as acute or subacute central vision loss leading to central scotoma and blindness. The disease has been associated with missense mutations in the mtDNA, in genes for Complex I, III, and IV polypeptides, that can act autonomously or in association with each other to cause the disease. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim/, MIM#535000 (April 17, 2001)) - (Source - Diseases Database)

Leber optic atrophy is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Leber optic atrophy, or a subtype of Leber optic atrophy, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

 

By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.

Home | Symptoms | Diseases | Diagnosis | Videos | Tools | Forum | About Us | Terms of Use | Privacy Policy | Site Map | Advertise