Connexin 26 (GJB2) mutation in an Argentinean patient with keratitis-ichthyosis-deafness (KID) syndrome: a case report-Reference-Cited by-同舟云学术

Connexin 26 (GJB2) mutation in an Argentinean patient with keratitis-ichthyosis-deafness (KID) syndrome: a case report

Published:2016-05-04 Issue:1 Volume:17 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Dalamón Viviana Karina,Buonfiglio Paula,Larralde Margarita,Craig Patricio,Lotersztein Vanesa,Choate Keith,Pallares Norma,Diamante Vicente,Elgoyhen Ana Belén

Funder

ANPCyT

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/s12881-016-0298-y

Reference44 articles.

1. Alli N, Gungor E. Keratitis, ichthyosis and deafness (KID) syndrome. Int J Dermatol. 1997;36(1):37–40.

2. Caceres-Rios H et al. Keratitis, ichthyosis, and deafness (KID syndrome): review of the literature and proposal of a new terminology. Pediatr Dermatol. 1996;13(2):105–13.

3. Langer K, Konrad K, Wolff K. Keratitis, ichthyosis and deafness (KID)-syndrome: report of three cases and a review of the literature. Br J Dermatol. 1990;122(5):689–97.

4. Grob JJ et al. Keratitis, ichthyosis, and deafness (KID) syndrome. Vertical transmission and death from multiple squamous cell carcinomas. Arch Dermatol. 1987;123(6):777–82.

5. Hazen PG et al. Keratitis, ichthyosis, and deafness (KID) syndrome: management with chronic oral ketoconazole therapy. Int J Dermatol. 1992;31(1):58–9.

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