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Year Number of Results
1986 1
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1989 2
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1995 1
1996 1
2000 1
2002 7
2003 4
2004 1
2005 5
2006 5
2007 7
2008 6
2009 5
2010 8
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2012 10
2013 9
2014 10
2015 8
2016 7
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146 results

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Page 1
Clinical, etiopathogenic, and therapeutic aspects of KID syndrome.
Cammarata-Scalisi F, Willoughby CE, Cárdenas Tadich A, Labrador N, Herrera A, Callea M. Cammarata-Scalisi F, et al. Dermatol Ther. 2020 Jul;33(4):e13507. doi: 10.1111/dth.13507. Epub 2020 Jul 4. Dermatol Ther. 2020. PMID: 32367610 Review.
Keratitis-ichthyosis-deafness (KID syndrome) is a syndromes ichthyoses that is clinically and genetically heterogeneous requiring early and long-term multidisciplinary monitoring of affected individuals. ...
Keratitis-ichthyosis-deafness (KID syndrome) is a syndromes ichthyoses that is clinically and genetically …
[Keratitis-ichthyosis-deafness (KID) syndrome].
Mazereeuw-Hautier J. Mazereeuw-Hautier J. Ann Dermatol Venereol. 2008 Jan;135(1):80-2; quiz 79, 83. doi: 10.1016/j.annder.2007.11.013. Epub 2008 Jan 24. Ann Dermatol Venereol. 2008. PMID: 18342082 Review. French. No abstract available.
Keratitis-ichthyosis-deafness (KID) syndrome.
Gonzalez ME, Tlougan BE, Price HN, Patel R, Kamino H, Schaffer JV. Gonzalez ME, et al. Dermatol Online J. 2009 Aug 15;15(8):11. Dermatol Online J. 2009. PMID: 19891919 Free article.
These skin findings were accompanied by sensorineural hearing loss and keratoconjunctivitis, a clinical triad diagnostic of keratitis-ichthyosis-deafness (KID) syndrome. The patient also had a history of recurrent infections and cysts on the sca …
These skin findings were accompanied by sensorineural hearing loss and keratoconjunctivitis, a clinical triad diagnostic of keratitis …
Keratitis-ichthyosis-deafness syndrome and hidradenitis suppurativa.
Travis L, Ou Yang J, Andersen RK, Skovby F, Jemec GBE, Saunte DM. Travis L, et al. JAAD Case Rep. 2023 Jun 15;38:158-162. doi: 10.1016/j.jdcr.2023.06.003. eCollection 2023 Aug. JAAD Case Rep. 2023. PMID: 37555193 Free PMC article. No abstract available.
Hidradenitis suppurrativa (acne inversa) as a systemic disease.
Dessinioti C, Katsambas A, Antoniou C. Dessinioti C, et al. Clin Dermatol. 2014 May-Jun;32(3):397-408. doi: 10.1016/j.clindermatol.2013.11.006. Epub 2013 Nov 22. Clin Dermatol. 2014. PMID: 24767187 Review.
There are several reports in the literature of the coexistence of HS with other diseases, including pyoderma gangrenosum, PASH syndrome, Adamantiades-Behcet's disease, spondylarthropathy, Crohn's disease, SAPHO, pachyonychia congenita, Dowling-Degos disease, and the ker …
There are several reports in the literature of the coexistence of HS with other diseases, including pyoderma gangrenosum, PASH syndrome …
Antibody gene transfer treatment drastically improves epidermal pathology in a keratitis ichthyosis deafness syndrome model using male mice.
Peres C, Sellitto C, Nardin C, Putti S, Orsini T, Di Pietro C, Marazziti D, Vitiello A, Calistri A, Rigamonti M, Scavizzi F, Raspa M, Zonta F, Yang G, White TW, Mammano F. Peres C, et al. EBioMedicine. 2023 Mar;89:104453. doi: 10.1016/j.ebiom.2023.104453. Epub 2023 Feb 1. EBioMedicine. 2023. PMID: 36736132 Free PMC article.
BACKGROUND: Keratitis ichthyosis deafness (KID) syndrome is a rare disorder caused by hemichannel (HC) activating gain-of-function mutations in the GJB2 gene encoding connexin (Cx) 26, for which there is no cure, or current treatments based upon …
BACKGROUND: Keratitis ichthyosis deafness (KID) syndrome is a rare disorder caused by hemichannel (HC) ac …
Keratitis-ichthyosis-deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patients.
Mazereeuw-Hautier J, Bitoun E, Chevrant-Breton J, Man SY, Bodemer C, Prins C, Antille C, Saurat JH, Atherton D, Harper JI, Kelsell DP, Hovnanian A. Mazereeuw-Hautier J, et al. Br J Dermatol. 2007 May;156(5):1015-9. doi: 10.1111/j.1365-2133.2007.07806.x. Epub 2007 Mar 23. Br J Dermatol. 2007. PMID: 17381453 Review.
BACKGROUND: Keratitis-ichthyosis-deafness (KID) syndrome is a rare congenital disorder characterized by the association of skin lesions, hearing loss and vascularizing keratitis. KID syndrome is caused by autosomal dominant mutatio …
BACKGROUND: Keratitis-ichthyosis-deafness (KID) syndrome is a rare congenital disorder characterized by t …
Malignant skin tumours in patients with inherited ichthyosis.
Natsuga K, Akiyama M, Shimizu H. Natsuga K, et al. Br J Dermatol. 2011 Aug;165(2):263-8. doi: 10.1111/j.1365-2133.2011.10381.x. Epub 2011 Jul 11. Br J Dermatol. 2011. PMID: 21517795 Review.
A survey of the literature revealed 28 cases of inherited ichthyoses with skin malignancy, including 12 cases of keratitis-ichthyosis-deafness (KID) syndrome, seven of autosomal recessive congenital ichthyosis, three of Netherton syndrome …
A survey of the literature revealed 28 cases of inherited ichthyoses with skin malignancy, including 12 cases of keratitis-ichthyo …
Antenatal Findings of Keratitis-Ichthyosis-Deafness Syndrome.
Okmen F, Hortu I, Jafarova U, Imamoglu M, Ekici H, Ergenoglu AM. Okmen F, et al. J Obstet Gynaecol Can. 2020 Apr;42(4):504-506. doi: 10.1016/j.jogc.2019.06.005. Epub 2019 Aug 14. J Obstet Gynaecol Can. 2020. PMID: 31421982
BACKGROUND: Keratitis-ichthyosis-deafness (KID) syndrome is a congenital ectodermal disorder characterized by keratitis, ichthyosis, and deafness. This syndrome affects multiple systems and can be fatal. CASE: A 34-year-old G2, P1 woman w …
BACKGROUND: Keratitis-ichthyosis-deafness (KID) syndrome is a congenital ectodermal disorder characterize …
From Hyperactive Connexin26 Hemichannels to Impairments in Epidermal Calcium Gradient and Permeability Barrier in the Keratitis-Ichthyosis-Deafness Syndrome.
García IE, Bosen F, Mujica P, Pupo A, Flores-Muñoz C, Jara O, González C, Willecke K, Martínez AD. García IE, et al. J Invest Dermatol. 2016 Mar;136(3):574-583. doi: 10.1016/j.jid.2015.11.017. Epub 2016 Jan 8. J Invest Dermatol. 2016. PMID: 26777423 Free article. Review.
The keratitis-ichthyosis-deafness (KID) syndrome is characterized by corneal, skin, and hearing abnormalities. ...Here we have compiled relevant data regarding the KID syndrome and propose a mechanism for the epidermal aspects of t …
The keratitis-ichthyosis-deafness (KID) syndrome is characterized by corneal, skin, and hearing abnormali …
146 results