Ocular Surface Stem Cell Transplantation for Treatment of Keratitis–Ichthyosis–Deafness Syndrome

Author:

Cheung Albert Y.,Patel Sunny,Kurji Khaliq H.,Sarnicola Enrica,Eslani Medi,Govil Amit,Holland Edward J.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Ophthalmology

Reference13 articles.

1. A case of generalized congenital keratoderma, with unusual involvement of the eyes, ears, and nasal and buccal mucous membranes;Burns;J Cutan Dis.,1915

2. The keratitis, ichthyosis, and deafness (KID) syndrome;Skinner;Arch Dermatol.,1981

3. Ocular manifestations of keratitis-ichthyosis-deafness (KID) syndrome;Messmer;Ophthalmology.,2005

4. Keratitis, hepatitis, ichthyosis, and deafness: report and review of KID syndrome;Wilson;Am J Med Genet.,1991

5. De novo mutation in the gene encoding connexin-26 (GJB2) in a sporadic case of keratitis-ichthyosis-deafness (KID) syndrome;Alvarez;Am J Med Genet.,2003

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