Related Experiment Video
Updated: Jul 5, 2026
Quantitative Fundus Autofluorescence for the Evaluation of Retinal Diseases
Published on: March 11, 2016
Expanding the Clinical and Genetic Spectrum of TTLL5-Associated Retinal Dystrophy: A Single-Center Cohort Study
Yunyu Zhou1, Yue Liu1, Huan Chen1
1Department of Ophthalmology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Purpose:
To characterize the clinical and genetic spectrum of TTLL5-related retinal dystrophy.
Design:
Retrospective observational study.
Subjects:
Twenty-one affected individuals from 19 unrelated families carrying biallelic TTLL5 variants.
Methods:
Patients with inherited retinal dystrophy and confirmed biallelic TTLL5 variants were retrospectively reviewed. Genetic diagnosis was established using whole-exome sequencing followed by Sanger confirmation and cosegregation analysis. Clinical assessments included best-corrected visual acuity, multimodal retinal imaging, visual field testing, and full-field electroretinography.
Main Outcome Measures:
Visual function, retinal structural and functional characteristics, and genotype-phenotype correlation.
Results:
The cohort included 10 males and 11 females, aged 6 to 66 years. Based on phenotypic classification, 2 patients were diagnosed with cone dystrophy (CD), 12 with cone-rod dystrophy (CRD), and 7 with rod-cone dystrophy (RCD). Best-corrected visual acuity ranged from 0 to 2.70 logarithm of the minimum angle of resolution (LogMAR) (median, 0.6 LogMAR; interquartile range, 1.55) and was significantly correlated with age (Spearman R = 0.704; P < 0.001). All patients were myopic, with spherical equivalent values ranging from -1.13 to -18.00 diopters, and 14 of 21 (66.67%) had bilateral high myopia (≤-6.0 diopters). Retinal involvement was characterized by macular degeneration with progressive extension beyond the posterior pole. Fundus autofluorescence demonstrated parafoveal or macular hyperautofluorescent rings followed by expanding hypoautofluorescent areas, whereas OCT revealed parafoveal-to-diffuse disruption or loss of the ellipsoid zone with outer nuclear layer thinning. Genetic analysis identified 24 pathogenic variants, of which 19 (79.17%) were novel. The recurrent missense variant c.437G>A (p.Gly146Glu) was the most frequent allele in this cohort and was consistently associated with a CRD phenotype. Extraocular manifestations were uncommon, with sensorineural hearing loss observed in 1 patient.
Conclusions:
TTLL5-associated retinal dystrophy exhibits a broad clinical spectrum encompassing CD, CRD, and RCD, with a high prevalence of myopia as a shared feature. The recurrent p.Gly146Glu variant showed a consistent association with the CRD phenotype, suggesting specific allele-phenotype correlations. These findings expand the recognized phenotypic and genetic spectrum of TTLL5-related disease and provide an important clinical framework for diagnosis, counseling, natural history, and future therapeutic studies.
Financial Disclosure(S):
The authors have no proprietary or commercial interest in any materials discussed in this article.
Related Concept Videos
01:20The Retinoblastoma Gene
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...
01:20The Retinoblastoma Gene
The first-ever tumor suppressor gene called Rb was identified in retinoblastoma - a rare eye tumor in children. In inherited forms of the disease, a child inherits one defective copy of the Rb gene, which predisposes them to retinoblastoma. However,...