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Last Updated: 02/24/2026

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Found 190 publications

Cranial osteomyelitis in a patient with KID syndrome: Importance of thorough investigation in chronic wounds.

Cranial osteomyelitis in a patient with KID syndrome: Importance of thorough investigation in chronic wounds.

Journal: Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG
Published: June 24, 2025

Expanding the clinical spectrum: A case report of the first Jordanian presentation of KID syndrome with neurological and skeletal anomalies beyond the classical triad.

Expanding the clinical spectrum: A case report of the first Jordanian presentation of KID syndrome with neurological and skeletal anomalies beyond the classical triad.

Journal: Medicine
Published: May 07, 2025

Genotype-Phenotype Correlations, Mortality, and Clinical Insights in Keratitis-Ichthyosis-Deafness Syndrome: A Comprehensive Review and Case Report.

Genotype-Phenotype Correlations, Mortality, and Clinical Insights in Keratitis-Ichthyosis-Deafness Syndrome: A Comprehensive Review and Case Report.

Journal: American journal of medical genetics. Part A
Published: March 01, 2025

Ophthalmologic management in KID syndrome: Long-term clinical experience.

Ophthalmologic management in KID syndrome: Long-term clinical experience.

Journal: Archivos de la Sociedad Espanola de Oftalmologia
Published: February 05, 2025

Hypodontia in a child with keratitis-ichthyosis-deafness (KID) syndrome: a case report.

Hypodontia in a child with keratitis-ichthyosis-deafness (KID) syndrome: a case report.

Journal: Journal of medical case reports
Published: January 25, 2025

Keratitis, Ichthyosis, and Deafness Syndrome with Endocarditis and Myelitis: A Rare Case Report.

Keratitis, Ichthyosis, and Deafness Syndrome with Endocarditis and Myelitis: A Rare Case Report.

Journal: Case reports in dermatology
Published: January 18, 2025

Clinical, biochemical and cell biological characterization of KIDAR syndrome associated with a novel AP1B1 variant.

Clinical, biochemical and cell biological characterization of KIDAR syndrome associated with a novel AP1B1 variant.

Journal: Molecular genetics and metabolism
Published: December 09, 2024

Dental Abnormalities in Congenital Ichthyoses: Case Report and Review of the Literature.

Dental Abnormalities in Congenital Ichthyoses: Case Report and Review of the Literature.

Journal: Pediatric dermatology
Published: July 29, 2024

Ocular phenotype and therapeutic interventions in keratitis-ichthyosis-deafness (KID) syndrome.

Ocular phenotype and therapeutic interventions in keratitis-ichthyosis-deafness (KID) syndrome.

Journal: Ophthalmic genetics
Published: September 27, 2023

Emergence of multiple revertant keratinocyte clones in a patient with KID syndrome.

Emergence of multiple revertant keratinocyte clones in a patient with KID syndrome.

Journal: Journal of the European Academy of Dermatology and Venereology : JEADV
Published: July 05, 2023

Expression of KID syndromic mutation Cx26S17F produces hyperactive hemichannels in supporting cells of the organ of Corti.

Expression of KID syndromic mutation Cx26S17F produces hyperactive hemichannels in supporting cells of the organ of Corti.

Journal: Frontiers in cell and developmental biology
Published: October 15, 2022

Antibody gene transfer treatment drastically improves epidermal pathology in a keratitis ichthyosis deafness syndrome model using male mice.

Antibody gene transfer treatment drastically improves epidermal pathology in a keratitis ichthyosis deafness syndrome model using male mice.

Journal: EBioMedicine
Published: September 23, 2022
Showing 1-12 of 190

Last Updated: 02/24/2026