AI Article Synopsis

  • The study aimed to analyze the clinical and genetic features of patients with -associated retinal disorders (-RD) by examining a group of 15 patients from 12 families.
  • Comprehensive eye exams were conducted to classify the patients into three subgroups: macular dystrophy (MD), cone-rod dystrophy (CORD), and Leber congenital amaurosis (LCA), while also assessing genetic variants.
  • Results showed a diverse range of symptoms and severities, with findings that suggest a lower prevalence of certain retinal disorders in the Japanese population, providing valuable data for patient counseling and future treatment strategies.

Article Abstract

Purpose: To determine the clinical and genetic characteristics of patients with -associated retinal disorder (-RD).

Methods: Fifteen patients from 12 families with inherited retinal disorder (IRD) and harboring variants were ascertained from 730 Japanese families with IRD. Comprehensive ophthalmological examinations, including visual acuity (VA) measurement, retinal imaging, and electrophysiological assessment were performed to classify patients into three phenotype subgroups; macular dystrophy (MD), cone-rod dystrophy (CORD), and Leber congenital amaurosis (LCA). In silico analysis was performed for the detected variants, and the molecularly confirmed inheritance pattern was determined (autosomal dominant/recessive [AD/AR]).

Results: The median age of onset/examination was 22.0/38.0 years (ranges, 0-55 and 1-73) with a median VA of 0.80/0.70 LogMAR units (ranges, 0.00-1.52 and 0.10-1.52) in the right/left eye, respectively. Macular atrophy was identified in seven patients (46.7%), and two had diffuse fundus disturbance (13.3%), and six had an essentially normal fundus (40.0%). There were 11 patients with generalized cone-rod dysfunction (78.6%), two with entire functional loss (14.3%), and one with confined macular dysfunction (7.1%). There were nine families with ADCORD, one with ARCORD, one with ADMD, and one with ARLCA. Ten variants were identified, including four novel variants (p.Val56GlyfsTer262, p.Met246Ile, p.Arg761Trp, p.Glu874Lys).

Conclusions: This large cohort study delineates the disease spectrum of -RD. Diverse clinical presentations with various severities of ADCORD and the early-onset severe phenotype of ARLCA are illustrated. A relatively lower prevalence of -RD for ADCORD and ARLCA in the Japanese population was revealed.

Translational Relevance: The obtained data help to monitor and counsel patients, especially in East Asia, as well as to design future therapeutic approaches.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408927PMC
http://dx.doi.org/10.1167/tvst.9.6.2DOI Listing

Publication Analysis

Top Keywords

retinal disorder
12
clinical genetic
8
genetic characteristics
8
characteristics patients
8
japanese families
8
-associated retinal
8
patients
7
patients japanese
4
families
4
families -associated
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!