The site of the Media Sphera Publishers contains materials intended solely for healthcare professionals.
By closing this message, you confirm that you are a certified medical professional or a student of a medical educational institution.

Korolenkova M.V.

Central Research Institute of Dentistry and Maxillofacial Surgery, Moscow

Dmitrieva N.A.

Babichenko I.I.

Russian University of People’s Friendship, Moscow, Russia, 117198

Gusova Yu.V.

Central Research Institute of Dentistry and Maxillofacial Surgery, Moscow, Russia

Poberezhnaya A.A.

Central Research Institute of Dentistry and Maxillofacial Surgery, Moscow, Russia

Oral manifestations of KID syndrome: rare clinical case

Authors:

Korolenkova M.V., Dmitrieva N.A., Babichenko I.I., Gusova Yu.V., Poberezhnaya A.A.

More about the authors

Journal: Stomatology. 2019;98(4): 93‑95

Read: 1707 times


To cite this article:

Korolenkova MV, Dmitrieva NA, Babichenko II, Gusova YuV, Poberezhnaya AA. Oral manifestations of KID syndrome: rare clinical case. Stomatology. 2019;98(4):93‑95. (In Russ.)
https://doi.org/10.17116/stomat20199804193

Recommended articles:
Preoperative protective preparation of the nasal mucosa of rhinological patients. Russian Bulletin of Otorhinolaryngology. 2024;(5):23-28
Clinical Case of Tattoo Pigment Dete­ction in Sentinel Lymph Nodes Against the Background of Mela­noma. Russian Journal of Clinical Dermatology and Vene­reology. 2024;(6):679-683
Morphogenesis and mole­cular regu­lation of poly­posis rhinosinusitis. Russian Journal of Archive of Pathology. 2025;(1):68-76

References:

  1. Terrinoni A, Codispoti A, Serra V, Bruno E, Didona B, et al. Connexin 26 (GJB2) mutations as a cause of the KID syndrome with hearing loss. Biochem Biophys Res Commun. 2010;395(1):25-30. https://doi.org/10.1016/j.bbrc.2010.03.098
  2. Dalamón VK, Buonfiglio P, Larralde M, Craig P, Lotersztein V, et al. Connexin 26 (GJB2) mutation in an Argentinean patient with keratitis-ichthyosis-deafness (KID) syndrome: a case report. BMC Med Genet. 2016;17(1):37. https://doi.org/10.1186/s12881-016-0298-y
  3. Martin PE, Easton JA, Hodgins MB, Wright CS. Connexins: sensors of epidermal integrity that are therapeutic targets. FEBS Lett. 2014;588(8):1304-1314. https://doi.org/10.1016/j.febslet.2014.02.048
  4. Taki T, Takeichi T, Sugiura K, Akiyama M. Roles of aberrant hemichannel activities due to mutant connexin26 in the pathogenesis of KID syndrome. Sci Rep. 2018;8(1):12824. https://doi.org/10.1038/s41598-018-30757-3
  5. Laird DW. Life cycle of connexins in health and disease. Biochem J. 2006;394:527-543.
  6. Brandner JM, Houdek P, Husing B, Kaiser C, Moll I. Connexins 26, 30, and 43: differences among spontaneous, chronic, and accelerated human wound healing. J Invest Dermatol. 2004;122:1310-1320.
  7. Labarthe MP, Bosco D, Saurat JH, Meda P, Salomon D. Upregulation of connexin 26 between keratinocytes of psoriatic lesions. J Invest Dermatol. 1998;111:72-76.
  8. Lucke T, Choudhry R, Thom R, Selmer IS, Burden AD, Hodgins MB. Upregulation of connexin 26 is a feature of keratinocyte differentiation in hyperproliferative epidermis, vaginal epithelium, and buccal epithelium. J Invest Dermatol. 1999;112:354-361.
  9. Tu CL, Crumrine DA, Man MQ, Chang W, Elalieh H, You M, Elias PM, Bikle DD. Ablation of the calcium-sensing receptor in keratinocytes impairs epidermal differentiation and barrier function. J Invest Dermatol. 2012;132:2350-2359.
  10. Kutkowska-Kaźmierczak A, Niepokój K, Wertheim-Tysarowska K, Giza A, Mordasewicz-Goliszewska M, Bal J, Obersztyn E. Phenotypic variability in gap junction syndromic skin disorders: experience from KID and Clouston syndromes’ clinical diagnostics. J Appl Genet. 2015;56(3):329-337. https://doi.org/10.1007/s13353-014-0266-1
  11. Bergman R, et al. KID syndrome: histopathological, immunohistochemical and molecular analysis of precancerous and cancerous skin lesions. Br J Dermatol. 2012;166(2):455-457. https://doi.org/10.1111/j.1365-2133.2011.10577.x
  12. Haruna K, Suga Y, Oizumi A, Mizuno Y, Endo H, Shimizu T, Hasegawa T, Ikeda S. Severe form of keratitis-ichthyosis-deafness (KID) syndrome associated with septic complications. J Dermatol. 2010;37(7):680-682. https://doi.org/10.1111/j.1346-8138.2010.00839.x
  13. Lai Y, Cogen AL, Radek KA, Park HJ, Macleod DT, Leichtle A, Ryan AF, Di Nardo A, Gallo RL. Activation of TLR2 by a small molecule produced by Staphylococcus epidermidis increases antimicrobial defense against bacterial skin infections. J Invest Dermatol. 2010;130(9):2211-2221. https://doi.org/10.1038/jid.2010.123

Email Confirmation

An email was sent to test@gmail.com with a confirmation link. Follow the link from the letter to complete the registration on the site.

Email Confirmation

We use cооkies to improve the performance of the site. By staying on our site, you agree to the terms of use of cооkies. To view our Privacy and Cookie Policy, please. click here.