[New techniques for quantification of color vision in disorders of cone function : Cambridge color test and photoreceptor-specific temporal contrast sensitivity in patients with heterozygous RP1L1 and RPGR mutations].
Cord HuchzermeyerJulien FarsHeidi StöhrJan KremersPublished in: Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft (2021)
The demonstration of dyschromatopsia is very helpful in the diagnosis of inherited retinal diseases, in addition to modern imaging techniques, such as optical coherence tomography (OCT) and fundus fluorescence. New functional techniques enable quantification of color vision disturbances and could be useful as outcome parameters in clinical trials of new gene and stem cell-based therapies.
Keyphrases
- optical coherence tomography
- diabetic retinopathy
- stem cells
- clinical trial
- optic nerve
- magnetic resonance
- early onset
- single molecule
- copy number
- magnetic resonance imaging
- randomized controlled trial
- transcription factor
- genome wide identification
- mesenchymal stem cells
- mass spectrometry
- cell therapy
- bone marrow
- phase ii
- fluorescence imaging
- phase iii
- photodynamic therapy