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Leber Hereditary Optic Neuropathy (LHON) Historical Case Record Survey

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Clinical Trial

NCT01892943 Completed
Leber Hereditary Optic Neuropathy (LHON) Historical Case Record Survey

Leber Hereditary Optic Neuropathy (LHON) Historical Case Record Survey.

Observational
Observational

Disease

Disease type

Paediatric clinical trials

Orphan drug recognition

NA

Patient type

Adult

Children

Inclusion / Exclusion

Opening date

01/08/2013

Closing date

01/02/2014

Inclusion criteria :

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Exclusion criteria :

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Funding

industry

Members involved

Main investigators

Pr José-Alain Sahel

France

Genetic Diagnostics (TWG6), Low Vision Daily Life and Patients Groups (TWG5), Neuro-Ophthalmology Rare Diseases (WG2), Pediatric Ophthalmology Rare Diseases (WG3), Registries & Epidemiology (TWG7), Research (TWG8), Retinal Rare Eye Diseases (WG1)
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ERN EYE member investigating site

HCP : Principal investigators