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9. [Keratitis-ichthyosis-deafness (KID) syndrome: an observation in a child in sub-Saharan Africa]. Barruet K; Saka B; Kombaté K; Mouhari-Toure A; Nguepmeni Noune J; Akakpo S; Tchangaï-Walla K; Pitché P Ann Dermatol Venereol; 2011 May; 138(5):453-5. PubMed ID: 21570577 [No Abstract] [Full Text] [Related]
10. [KID syndrome (keratitis-ichthyosis-deafness)]. Puig L; Moreno A; Perez M; De Moragas JM Med Cutan Ibero Lat Am; 1987; 15(3):223-8. PubMed ID: 3312867 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. [KID syndrome (keratitis, ichthyosis and deafness)]. André N; Koné-Paut I; Koeppel MC; Berbis P Arch Pediatr; 1999 Mar; 6(3):302-6. PubMed ID: 10191899 [TBL] [Abstract][Full Text] [Related]
14. Additional aspects of keratitis, ichthyosis, and deafness (KID) syndrome. Möhrenschlager M; Ring J; Abeck D Pediatr Dermatol; 2004; 21(4):518-9; author reply 519. PubMed ID: 15283813 [No Abstract] [Full Text] [Related]
15. Surgical therapy in a patient with Keratosis-Ichthyosis-Deafness (KID) syndrome associated with follicular occlusion triad. Wenghoefer M; Allam JP; Novak N; Maintz L; Martini M; Bergé S Eur J Dermatol; 2007; 17(5):449-50. PubMed ID: 17673397 [No Abstract] [Full Text] [Related]
16. 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]
17. A congenital ichthyosiform syndrome with deafness and keratitis. Cram DL; Resneck JS; Jackson WB Arch Dermatol; 1979 Apr; 115(4):467-71. PubMed ID: 434873 [TBL] [Abstract][Full Text] [Related]
18. [Dry congenital erythroderma ichthyosiforme, deaf-mutism, and hypetomegaly, of recessive autosome transmission. Study of a family]. Desmons F; Bar J; Chevillard Y Bull Soc Fr Dermatol Syphiligr; 1971; 78(6):585-91. PubMed ID: 4119872 [No Abstract] [Full Text] [Related]