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KID Syndrome: A Rare Genodermatosis.

作者信息

Dey Vivek Kumar, Saxena Animesh, Parikh Shrini

机构信息

Department of Dermatology, People's College of Medial Sciences and Research Centre, Bhopal, Madhya Pradesh, India.

出版信息

Indian Dermatol Online J. 2020 Jan 13;11(1):116-118. doi: 10.4103/idoj.IDOJ_87_19. eCollection 2020 Jan-Feb.

DOI:10.4103/idoj.IDOJ_87_19
PMID:32055527
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7001397/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62f8/7001397/1c801e62c84e/IDOJ-11-116-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62f8/7001397/5064552a8ec1/IDOJ-11-116-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62f8/7001397/4e639d0f355e/IDOJ-11-116-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62f8/7001397/6b592698ef3b/IDOJ-11-116-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62f8/7001397/1c801e62c84e/IDOJ-11-116-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62f8/7001397/5064552a8ec1/IDOJ-11-116-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62f8/7001397/4e639d0f355e/IDOJ-11-116-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62f8/7001397/6b592698ef3b/IDOJ-11-116-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62f8/7001397/1c801e62c84e/IDOJ-11-116-g004.jpg

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引用本文的文献

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Novel Variant c.148G>T of GJB2 Gene in a 5-Year-Old Child with KID Syndrome.一名患有KID综合征的5岁儿童中GJB2基因的新型c.148G>T变异
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本文引用的文献

1
Visual impairment reversal with oral acitretin therapy in keratitis-ichthyosis-deafness (KID) syndrome.口服阿维A治疗角膜炎-鱼鳞病-耳聋（KID）综合征实现视力障碍逆转
JAAD Case Rep. 2017 Nov 8;3(6):556-558. doi: 10.1016/j.jdcr.2017.07.021. eCollection 2017 Nov.
2
Severe Phenotype of Keratitis-Ichthyosis-Deafness Syndrome With Presumed Ocular Surface Squamous Neoplasia.伴有疑似眼表鳞状上皮肿瘤的角膜炎-鱼鳞病-耳聋综合征的严重表型
Cornea. 2018 Feb;37(2):252-254. doi: 10.1097/ICO.0000000000001387.
3
Keratitis-ichthyosis-deafness syndrome: first affected family reported in the Middle East.
角膜炎-鱼鳞病-耳聋综合征：中东地区首次报道的受累家庭。
Int Med Case Rep J. 2014 Mar 25;7:63-6. doi: 10.2147/IMCRJ.S58432. eCollection 2014.
4
[Diagnostics of keratitis-ichthyosis-deafness syndrome (KID- syndrome)].
Vestn Otorinolaringol. 2012(3):58-61.
5
GJB2 Gene Mutations in Syndromic Skin Diseases with Sensorineural Hearing Loss.GJB2 基因突变与综合征型皮肤疾病伴神经性耳聋
Curr Genomics. 2011 Nov;12(7):475-785. doi: 10.2174/138920211797904098.
6
Keratitis-ichthyosis-deafness (KID) syndrome.
Dermatol Online J. 2009 Aug 15;15(8):11.
7
A report of GJB2 (N14K) Connexin 26 mutation in two patients--a new subtype of KID syndrome?两名患者中GJB2（N14K）连接蛋白26突变的报告——一种KID综合征的新亚型？
Pediatr Dermatol. 2008 Sep-Oct;25(5):535-40. doi: 10.1111/j.1525-1470.2008.00767.x.
8
Keratitis-ichthyosis-deafness syndrome in association with follicular occlusion triad.角膜炎-鱼鳞病-耳聋综合征合并毛囊闭锁三联征。
Eur J Dermatol. 2005 Sep-Oct;15(5):347-52.
9
The keratitis, ichthyosis, and deafness (KID) syndrome.角膜炎、鱼鳞病和耳聋（KID）综合征
Arch Dermatol. 1981 May;117(5):285-9.
10
Familial occurrence of KID (keratitis, ichthyosis, deafness) syndrome. Case reports of a mother and daughter.KID（角膜炎、鱼鳞病、耳聋）综合征的家族性发病。一位母亲和女儿的病例报告。
J Am Acad Dermatol. 1990 Aug;23(2 Pt 2):385-8. doi: 10.1016/0190-9622(90)70229-b.