Familial Deafness Latest Advances

Find the Latest Research About Familial Deafness

Last Updated: 02/24/2026

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Found 886 publications

Gene therapy for hereditary deafness: progress, achievements and future challenges.

Gene therapy for hereditary deafness: progress, achievements and future challenges.

Journal: Acta oto-laryngologica
Published: January 06, 2026

Interpretation of the"Expert consensus on clinical practice for pre-pregnancy and prenatal prevention of hereditary hearing loss"

Interpretation of the"Expert consensus on clinical practice for pre-pregnancy and prenatal prevention of hereditary hearing loss"

Journal: Zhonghua yi xue za zhi
Published: October 26, 2025

The TECTB-C225Y Variant Causing Autosomal Dominant Deafness in a Nicaraguan Family Enhances Sensitivity to Noise-Induced Hearing Loss in Mice.

The TECTB-C225Y Variant Causing Autosomal Dominant Deafness in a Nicaraguan Family Enhances Sensitivity to Noise-Induced Hearing Loss in Mice.

Journal: medRxiv : the preprint server for health sciences
Published: August 20, 2025

Calcium blockers protect against sensory epithelial damage and hearing loss in Cx26-cKO mice.

Calcium blockers protect against sensory epithelial damage and hearing loss in Cx26-cKO mice.

Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Published: August 13, 2025

Establishing a comprehensive national auditory implant registry in Japan: Trends and demographics from the first two years (2023-2024).

Establishing a comprehensive national auditory implant registry in Japan: Trends and demographics from the first two years (2023-2024).

Journal: Auris, nasus, larynx
Published: August 04, 2025

Analysis of deafness gene screening results in 15771 newborn cases in Anyang city of Henan.

Analysis of deafness gene screening results in 15771 newborn cases in Anyang city of Henan.

Journal: Frontiers in pediatrics
Published: July 21, 2025

TMC1 and TMC2 are cholesterol-dependent scramblases that regulate membrane homeostasis in auditory hair cells.

TMC1 and TMC2 are cholesterol-dependent scramblases that regulate membrane homeostasis in auditory hair cells.

Journal: bioRxiv : the preprint server for biology
Published: July 09, 2025

Promotion of a new gap junction gene Cx46 (GJA3) expression in the cochlea after Cx26 (GJB2) deficiency.

Promotion of a new gap junction gene Cx46 (GJA3) expression in the cochlea after Cx26 (GJB2) deficiency.

Journal: Hearing research
Published: July 04, 2025

Hyperkinetic Movement Disorder in KARS1-Related Disease: An Illustrative Video-Recorded Case and Narrative Literature Review.

Hyperkinetic Movement Disorder in KARS1-Related Disease: An Illustrative Video-Recorded Case and Narrative Literature Review.

Journal: Neurology international
Published: June 28, 2025

Adeno-associated virus-based rescue of Myo7a expression restores hair-cell function and improves hearing thresholds in a USH1B mouse strain.

Adeno-associated virus-based rescue of Myo7a expression restores hair-cell function and improves hearing thresholds in a USH1B mouse strain.

Journal: The Journal of physiology
Published: June 18, 2025

The predawn dilemma in adeno-associated virus-based gene therapies for hereditary deafness.

The predawn dilemma in adeno-associated virus-based gene therapies for hereditary deafness.

Journal: American journal of stem cells
Published: June 07, 2025

Cochlear inflammation in AAV-mediated gene therapy: serotype-dependent macrophage activation and promoter-driven immunogenicity.

Cochlear inflammation in AAV-mediated gene therapy: serotype-dependent macrophage activation and promoter-driven immunogenicity.

Journal: Acta oto-laryngologica
Published: May 03, 2025
Showing 1-12 of 886

Last Updated: 02/24/2026