Conditions / Genetic
Leber congenital amaurosis 7
info · Genetic · ICD-10: H35.5
A Leber congenital amaurosis that has_material_basis_in mutation in the CRX gene on chromosome 19q13.
Signs and symptoms
- Undetectable electroretinogram
- Nystagmus
- Visual impairment
- Keratoconus
- Cataract
- Pendular nystagmus
- Photophobia
Also known as: LCA7