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New research · Ophthalmology
Journal of medical genetics · 5d
Cross-sectionalJournal of medical genetics · 2026

Inherited retinal disease genes with dual inheritance patterns: insights from the IRD-PT registry.

Mariana Ferreira Francisco, Beatriz Gaspar, Rufino Silva … João Pedro Marques
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OphthalmologyCross-sectional

Genes with both recessive and dominant inheritance caused 12% of inherited retinal disease diagnoses.

Inherited retinal disease genes with dual inheritance patterns: insights from the IRD-PT registry.

Mariana Ferreira Francisco … João Pedro Marques
Journal of medical genetics · 2026
Background

Inherited retinal diseases (inherited retinal diseases) typically follow a single inheritance pattern, but some genes cause disease through both autosomal recessive (autosomal recessive) and autosomal dominant (autosomal dominant) patterns, challenging genetic counselling.

Purpose

This study aims to identify dual inheritance genes in a Portuguese cohort and characterise the prevalence of each inheritance mode and associated phenotypes.

Methods

Cross-sectional study at Portugal's largest inherited retinal diseases referral centre.

n = 141 patients
Results
12%
these genes carry both inheritance types, muddying genetic counseling in about 1 in 8 diagnoses
n = 141 patients
More results

PRPH2 (95.0% autosomal dominant) was associated with retinitis pigmentosa (retinitis pigmentosa) and macular dystrophies.

ABCC6 (91.3% autosomal recessive) was linked to pseudoxanthoma elasticum (pseudoxanthoma elasticum).

More results

BEST1 (91.7% autosomal dominant) mainly caused Best disease, while PROM1 (76.9% autosomal recessive) was linked to retinitis pigmentosa, macular dystrophy and cone-rod dystrophy.

PRPF31 (88.9% autosomal dominant) was exclusively associated with retinitis pigmentosa.

“
Conclusion · 1 of 2

Dual inheritance genes accounted for 12% of our genetic diagnoses. This spectrum, modulated by variant location and allele dosage, determines phenotypes and contributes to inherited retinal diseases heterogeneity.

Conclusion · 2 of 2

Deep phenotyping and comprehensive molecular diagnosis are essential for accurate genetic counselling and patient management.

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