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7. Keratitis-Ichthyosis-Deafness Syndrome: Early Death Caused by the GJB2 Mutation p.Gly12Arg. Godillot C; Severino-Freire M; Michaud V; Boralevi F; Labrèze C; Guigonis V; Onnis G; Morice-Picard F; Mazereeuw-Hautier J Acta Derm Venereol; 2019 Sep; 99(10):921-922. PubMed ID: 31099403 [No Abstract] [Full Text] [Related]
8. The keratitis, ichthyosis, and deafness (KID) syndrome. Skinner BA; Greist MC; Norins AL Arch Dermatol; 1981 May; 117(5):285-9. PubMed ID: 7224657 [TBL] [Abstract][Full Text] [Related]
9. Keratitis, hepatitis, ichthyosis, and deafness: report and review of KID syndrome. Wilson GN; Squires RH; Weinberg AG Am J Med Genet; 1991 Sep; 40(3):255-9. PubMed ID: 1951425 [TBL] [Abstract][Full Text] [Related]
10. A case of keratitis ichthyosis deafness (KID) syndrome associated with Dandy-Walker. Zhang XB; Li CX J Eur Acad Dermatol Venereol; 2007 May; 21(5):706-7. PubMed ID: 17448003 [No Abstract] [Full Text] [Related]
11. Heterozygous p.Asp50Asn mutation in the GJB2 gene in two Cameroonian patients with keratitis-ichthyosis-deafness (KID) syndrome. Wonkam A; Noubiap JJ; Bosch J; Dandara C; Toure GB BMC Med Genet; 2013 Aug; 14():81. PubMed ID: 23924173 [TBL] [Abstract][Full Text] [Related]
12. A hyperkeratotic linear lesion in a girl with KID syndrome. A further example of early allelic loss? Restano L; Cambiaghi S; Brusasco A; Tardini G; Caputo R Eur J Dermatol; 1999 Mar; 9(2):142-3. PubMed ID: 10066965 [No Abstract] [Full Text] [Related]
13. Keratitis-ichthyosis-deafness syndrome: Phenotypic heterogeneity and treatment perspective of patients with p.Asp50Asn GJB2 mutation. Asgari T; Naji M; Mansouri P; Mahmoudi H; Zabihi M; Youssefian L; Mahdavi M; Naraghi ZS; Zeinali S; Vahidnezhad H; Uitto J Dermatol Ther; 2020 Nov; 33(6):e14493. PubMed ID: 33136289 [TBL] [Abstract][Full Text] [Related]
14. [Successful topical cyclosporin A in the therapy of progressive vascularising keratitis in keratitis-ichthyosis-deafness (KID) syndrome (Senter syndrome)]. Derse M; Wannke E; Payer H; Rohrbach JM; Zierhut M Klin Monbl Augenheilkd; 2002 May; 219(5):383-6. PubMed ID: 12094324 [TBL] [Abstract][Full Text] [Related]
15. Germline mosaicism in keratitis-ichthyosis-deafness syndrome: pre-natal diagnosis in a familial lethal form. Sbidian E; Feldmann D; Bengoa J; Fraitag S; Abadie V; de Prost Y; Bodemer C; Hadj-Rabia S Clin Genet; 2010 Jun; 77(6):587-92. PubMed ID: 20412116 [TBL] [Abstract][Full Text] [Related]