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KID syndrome

Keratitis-ichthyosis-deafness syndrome, autosomal dominant
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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "KID syndrome" returned 0 free, full-text review articles. First 0 results:
Treatment of keratitis-ichthyosis- deafness (KID) syndrome in children: a case report and review of the literature.
Last Updated: Apr 02, 2015

Keratitis-ichthyosis-deafness (KID) syndrome is a rare hereditary cornification disorder resulting from mutations in connexin 26, a protein important for intercellular communication. In addition to the characteristic clinical triad of congenital bilateral sensorineural hearing loss, ...

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0 Free Review Articles 9 Review Articles

Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "KID syndrome" returned 0 free, full-text editorial articles. First 0 results:
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "KID syndrome" returned 15 free, full-text research articles. First few results:
Roles of aberrant hemichannel activities due to mutant connexin26 in the pathogenesis of KID syndrome.
Last Updated: Oct 29, 2019

Germline missense mutations in GJB2 encoding connexin (Cx) 26 have been found in keratitis, ichthyosis and deafness (KID) syndrome. We explored the effects of three mouse Cx26 mutants (Cx26-G12R, -G45E and -D50N) corresponding to KID syndrome-causative human mutants on hemichannel ...

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15 Free Research Articles 79 Research Articles