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http://purl.uniprot.org/citations/32681094http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/32681094http://www.w3.org/2000/01/rdf-schema#comment"

Purpose

To describe the clinical and electrophysiological features of adult-onset macular dystrophy, due to novel combinations of CDHR1 alleles, and compare the associated phenotypes with previous reports.

Methods

The clinical records of patients with macular dystrophy and biallelic variants in CDHR1 were reviewed. Data analysed included best corrected visual acuity (BCVA), fundus images: autofluorescence (AF) and optical coherence tomography (OCT); full field electroretinography (ERG) and pattern ERG (PERG).

Results

Seven patients from six pedigrees were ascertained. One patient was homozygous for a known synonymous variant p.(Pro261=), four were compound heterozygous for the p.(Pro261=) variant and a novel allele of CDHR1: p.(Gly188Ser), p.(Met1?), or p.(Val458Asp); one patient was compound heterozygous for two previously unreported variants: c.297+1G>T in trans with p.(Pro735Thr). The range of BCVA at the last clinic review was (6/5-6/60). Autofluorescence showed macular flecks of increased AF in mild cases and patches of reduced AF in severe cases. The OCT showed attenuation of the ellipsoid zone (EZ) in mild cases and loss of the EZ and the outer nuclear layer in severe cases; one patient had subfoveal hyporeflective region between the EZ and the retinal pigment epithelium. The full field ERG was normal or borderline subnormal in all cases, and the PERG was subnormal in mild cases or undetectable in severe cases.

Conclusions

This report corroborates previous observations that genotypes distinct from those causing pan-retinal dystrophy can cause a milder phenotype, predominantly affecting the macula, and expands the spectrum of these genotypes. The findings in this cohort suggest a potential macular susceptibility to mild perturbations of the photoreceptor cadherin."xsd:string
http://purl.uniprot.org/citations/32681094http://purl.org/dc/terms/identifier"doi:10.1038/s41433-020-1045-3"xsd:string
http://purl.uniprot.org/citations/32681094http://purl.uniprot.org/core/author"Webster A.R."xsd:string
http://purl.uniprot.org/citations/32681094http://purl.uniprot.org/core/author"Wright G."xsd:string
http://purl.uniprot.org/citations/32681094http://purl.uniprot.org/core/author"Arno G."xsd:string
http://purl.uniprot.org/citations/32681094http://purl.uniprot.org/core/author"Robson A.G."xsd:string
http://purl.uniprot.org/citations/32681094http://purl.uniprot.org/core/author"Michaelides M."xsd:string
http://purl.uniprot.org/citations/32681094http://purl.uniprot.org/core/author"Mahroo O.A."xsd:string
http://purl.uniprot.org/citations/32681094http://purl.uniprot.org/core/author"Ba-Abbad R."xsd:string
http://purl.uniprot.org/citations/32681094http://purl.uniprot.org/core/author"Schiff E."xsd:string
http://purl.uniprot.org/citations/32681094http://purl.uniprot.org/core/author"Duignan E.S."xsd:string
http://purl.uniprot.org/citations/32681094http://purl.uniprot.org/core/date"2021"xsd:gYear
http://purl.uniprot.org/citations/32681094http://purl.uniprot.org/core/name"Eye (Lond)"xsd:string
http://purl.uniprot.org/citations/32681094http://purl.uniprot.org/core/pages"1482-1489"xsd:string
http://purl.uniprot.org/citations/32681094http://purl.uniprot.org/core/title"A clinical study of patients with novel CDHR1 genotypes associated with late-onset macular dystrophy."xsd:string
http://purl.uniprot.org/citations/32681094http://purl.uniprot.org/core/volume"35"xsd:string
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