Familial Deafness Latest Advances

Find the Latest Research About Familial Deafness

Last Updated: 06/30/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 892 publications

Recent Progress in Mechanism-Based Therapies for GJB2-Related Hearing Loss.

Recent Progress in Mechanism-Based Therapies for GJB2-Related Hearing Loss.

Journal: International journal of molecular sciences
Published: April 13, 2026

Identification and characterization of a novel p. S390C variant in TMC1 in an autosomal recessive family with non-syndromic hearing loss.

Identification and characterization of a novel p. S390C variant in TMC1 in an autosomal recessive family with non-syndromic hearing loss.

Journal: Acta oto-laryngologica
Published: January 26, 2026

Gene Editing Technologies for Hereditary Hearing Loss: Prospects and Challenges.

Gene Editing Technologies for Hereditary Hearing Loss: Prospects and Challenges.

Journal: Neuroscience bulletin
Published: January 06, 2026

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

MYO6 and Heart: A Novel Variant in a Deaf Infant With Supraventricular Tachycardia.

MYO6 and Heart: A Novel Variant in a Deaf Infant With Supraventricular Tachycardia.

Journal: Molecular genetics & genomic medicine
Published: November 01, 2025

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

Evolutionary tuning of an auditory transduction channel.

Evolutionary tuning of an auditory transduction channel.

Journal: Current biology : CB
Published: October 23, 2025

Human promoter-driven AAV tools enable precision gene therapy targeting cochlear hair cells.

Human promoter-driven AAV tools enable precision gene therapy targeting cochlear hair cells.

Journal: Cell reports. Medicine
Published: October 03, 2025

Dysregulation of Serpinb6a-Gch1 axis contributes to DFNB91 deafness that is amendable to gene therapies.

Dysregulation of Serpinb6a-Gch1 axis contributes to DFNB91 deafness that is amendable to gene therapies.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: September 14, 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

Comprehensive genotype-phenotype correlation analysis in 11 509 neonates carrying common deafness-associated pathogenic variants.

Comprehensive genotype-phenotype correlation analysis in 11 509 neonates carrying common deafness-associated pathogenic variants.

Journal: Journal of medical genetics
Published: August 10, 2025
Showing 1-12 of 892

Last Updated: 06/30/2026