Neue Techniken zur Quantifizierung des Farbsinns bei Störungen der Zapfenfunktion

URN to cite this document:: urn:nbn:de:bvb:355-epub-508045
DOI to cite this document:: 10.5283/epub.50804

Huchzermeyer, Cord

; Fars, Julien

; Stöhr, Heidi ; Kremers, Jan

License: Creative Commons Attribution 4.0
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Date of publication of this fulltext: 11 Oct 2021 13:28

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Abstract

Background Inherited retinal diseases with cone dysfunction can be accompanied by severe visual loss and a marked loss of color vision despite relatively normal fundus appearance. Autosomal dominant occult macular dystrophy (RP1L1gene) and X-chromosomal retinitis pigmentosa (RPGRgene, including heterozygous female carriers) are important examples. New examination techniques enable ...