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Last Updated: 10/31/2025
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Found 188 publications
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
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
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.
Journal: Case reports in dermatology
Published: January 18, 2025
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.
Journal: Pediatric dermatology
Published: July 29, 2024
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.
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.
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.
Journal: EBioMedicine
Published: September 23, 2022
Keratitis-ichthyosis-deafness syndrome: A comprehensive review of cutaneous and systemic manifestations.
Journal: Pediatric dermatology
Published: June 13, 2022
Severe KIDAR syndrome caused by deletion in the AP1B1 gene: Report of a teenage patient and systematic review of the literature.
Journal: European journal of medical genetics
Published: February 20, 2022
Last Updated: 10/31/2025