Ocena morfologii plamki oraz funkcji narządu wzroku w przebiegu zespołu Ushera

Purpose: Retinitis pigmentosa (RP) is a set of heterogenous retinal diseases that affect primarily photoreceptors and retinal pigmented

epithelium. The Usher’s syndrome (RP associated with hearing impairment or loss), is responsible for about 10-20% of all cases.

We investigate macular morphology using spectral domain optical coherence tomography in correlation with visual function.

Material and methods: Two patients with Usher syndrome: a 13 years old girl and her 9 years old sister underwent comprehensive ophthalmological examination including: BCVA testing (Snellen charts), biomicroscopy of the anterior and posterior segment of the eye, electroretinography and SD-OCT scans of the macular region.

Results: BCVA was noticeable decreased in both eyes (Vod = 5/16, Vos = 5/16), of 13 years old patient, while it was slightly

diminished in her younger sister (Vod = 5/6, Vos = 5/6). In patient with visual deterioration a blue cone deficiency was found.

Central foveal thickness (CFT) and foveal outer segment/pigment epithelium thickness (FOSPET) was significantly reduced in

13 years old patient.

Conclusions: Spectral optical coherence tomography is a useful method to monitor morphological changes of the macula and

their progress in patients with retinitis pigmentosa in Usher’s syndrome.