Phenotype #0000333638

Individual ID 00444385
Associated disease OPA
Phenotype details see paper; ..., sudden and painless visual loss at young age, partial recovery and persistent central scotoma; 6y-low vision; 12y-headache
Diagnosis/Initial Leber’s hereditary optic neuropathy
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 06y
Phenotype/Onset low vision
Birth_Details -
MotorSkills -
Vision/Abnormality -
Hearing/Loss -
Eye/Optic_Disc -
Protein -
Brain/Imaging -
Eye/OCT -
Vision/Field -
Vision/Acuity -
Vision/Colour -
Habits -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2023-12-23 19:48:26 +01:00 (CET)
Date last edited N/A

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