Keratitis, Ichthyosis, and Deafness (KID) Syndrome
Author:
Affiliation:
1. Department of Dermatology and Venereology, Medical University, Sofia, Bulgaria
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology and Child Health
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1525-1470.2002.00222.x
Reference17 articles.
1. A case of generalized congenital erythroderma;Burns FS;J Cutan Dis,1915
2. The keratitis, ichthyosis, and deafness (KID) syndrome
3. Keratitis, Ichthyosis, and Deafness (KID Syndrome): Review of the Literature and Proposal of a New Terminology
4. Keratitis, ichthyosis, and deafness (KID) syndrome. Vertical transmission and death from multiple squamous cell carcinomas
5. Familial occurrence of KID (keratitis, ichthyosis, deafness) syndrome
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1. From Mendel to mycoses: Immuno‐genomic warfare at the human–fungus interface;Immunological Reviews;2023-12-08
2. Of Mycelium and Men: Inherent Human Susceptibility to Fungal Diseases;Pathogens;2023-03-14
3. Two Cases of Chronic Candidiasis in Keratitis–Ichthyosis–Deafness Syndrome;The American Journal of Dermatopathology;2018-10
4. Roles of aberrant hemichannel activities due to mutant connexin26 in the pathogenesis of KID syndrome;Scientific Reports;2018-08-27
5. Phenotype in a patient with p.D50N mutation in GJB2 gene resemble both KID and Clouston syndromes;International Journal of Pediatric Otorhinolaryngology;2016-02
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