ABSTRACT
AIM: To describe the clinical and molecular features of a novel, autosomal dominant RDH12-retinopathy. METHODS: Retrospective cross-sectional study. Twelve individuals from a four-generation British pedigree underwent ophthalmic examination, genotyping using next generation sequencing, including whole genome sequencing and multimodal retinal imaging including fundus photography, optical coherence tomography (OCT), autofluorescence imaging and adaptive optics (AO) scanning light ophthalmoscopy were performed. Visual electrophysiology was performed in a subset. RESULTS: Eight family members were confirmed as affected by genotyping heterozygous for RDH12 c.763delG. Visual acuity ranged from -0.1 to 0.2 logMAR. Affected individuals had constricted visual fields. A parafoveal and peripapillary ring of hyper-autofluorescence was seen initially, and with progression the area of perifoveal hypo-autofluorescence increased to involve the parafoveal area. Mild retinal thinning was identified on OCT imaging with reduction in both foveal total retinal and outer nuclear layer thickness. Cone densities along the temporal meridian were reduced in affected individuals compared with normative values at all temporal eccentricities studied. One individual with incomplete penetrance, was identified as clinically affected primarily on the basis of AO imaging. Full-field electroretinography demonstrated a rod-cone pattern of dysfunction and large-field pattern electroretinography identified peripheral macular dysfunction. CONCLUSIONS: This novel heterozygous variant RDH12 c.763delG is associated with a rod-cone dystrophy with variable expression. Determination of the degree of penetrance may depend on the modality employed to phenotypically characterise an individual. This rare and specific heterozygous (dominant) variant is predicted to result in a gain of function, that causes disease in a gene typically associated with biallelic (recessive) variants.
Subject(s)
Retinal Degeneration , Retinitis Pigmentosa , Alcohol Oxidoreductases/genetics , Cross-Sectional Studies , Electroretinography , Humans , Mutation , Pedigree , Phenotype , Retinitis Pigmentosa/diagnosis , Retinitis Pigmentosa/genetics , Retrospective Studies , Tomography, Optical CoherenceABSTRACT
AIMS: To quantitatively analyse cone photoreceptor matrices on images captured on an adaptive optics (AO) camera and assess their correlation to well-established parameters in the retinal histology literature. METHODS: High resolution retinal images were acquired from 10 healthy subjects, aged 20-35â years old, using an AO camera (rtx1, Imagine Eyes, France). Left eye images were captured at 5° of retinal eccentricity, temporal to the fovea for consistency. In three subjects, images were also acquired at 0, 2, 3, 5 and 7° retinal eccentricities. Cone photoreceptor density was calculated following manual and automated counting. Inter-photoreceptor distance was also calculated. Voronoi domain and power spectrum analyses were performed for all images. RESULTS: At 5° eccentricity, the cone density (cones/mm(2) mean±SD) was 15.3±1.4×10(3) (automated) and 13.9±1.0×10(3) (manual) and the mean inter-photoreceptor distance was 8.6±0.4â µm. Cone density decreased and inter-photoreceptor distance increased with increasing retinal eccentricity from 2 to 7°. A regular hexagonal cone photoreceptor mosaic pattern was seen at 2, 3 and 5° of retinal eccentricity. CONCLUSIONS: Imaging data acquired from the AO camera match cone density, intercone distance and show the known features of cone photoreceptor distribution in the pericentral retina as reported by histology, namely, decreasing density values from 2 to 7° of eccentricity and the hexagonal packing arrangement. This confirms that AO flood imaging provides reliable estimates of pericentral cone photoreceptor distribution in normal subjects.
Subject(s)
Optics and Photonics/methods , Photography/methods , Retina/anatomy & histology , Retinal Cone Photoreceptor Cells/cytology , Adult , Cell Count , Feasibility Studies , Female , Humans , Male , Ophthalmoscopy/methods , Visual Fields/physiology , Young AdultSubject(s)
Diagnostic Imaging , Retinal Cone Photoreceptor Cells/cytology , Retinal Pigment Epithelium/transplantation , Wet Macular Degeneration/surgery , Aged , Aged, 80 and over , Cell Count , Cell Survival/physiology , Female , Humans , Photography/instrumentation , Retina/physiology , Tomography, Optical Coherence , Visual Acuity/physiology , Visual Field TestsABSTRACT
Sudden onset nonaxial proptosis and diplopia is alarming and orbital haemorrhage or a rapidly expanding orbital tumour should be excluded. We present a case of a young man aged 15 years who attended the Accident and Emergency Department with a 6-h history of sudden onset proptosis and diplopia in whom the aetiology was orbital emphysema.