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儿童鱼鳞病样红皮病综合征

KID syndrome.

作者信息

Abdollahi Ali, Hallaji Zahra, Esmaili Nafiseh, Valikhani Mahin, Barzegari Masoumeh, Akhyani Maryam, Toosi Siavash, Miresmaili Alireza

机构信息

Department of Ophthalmology, Farabi Hospital, Tehran University of Medical Sciences.

出版信息

Dermatol Online J. 2007 Oct 13;13(4):11.

PMID:18319008
Abstract

KID syndrome is a rare congenital disorder characterized by keratitis, ichthyosis, and deafness. We have described a 4-year-old girl who is treated with bland emollients and topical keratolytics such as urea and surprisingly observed marked improvement in skin hyperkeratosis and palmoplantar keratoderma. We think that along with urgent ophthalmologic and otolaryngologic measures, simple topical therapies may improve skin condition in KID syndrome precluding the possible hazards of systemic retinoid therapy.

摘要

KID综合征是一种罕见的先天性疾病,其特征为角膜炎、鱼鳞病和耳聋。我们描述了一名4岁女孩,她接受了温和润肤剂和尿素等外用角质松解剂的治疗,令人惊讶的是,皮肤过度角化和掌跖角皮病有明显改善。我们认为,除了紧急的眼科和耳鼻喉科措施外,简单的局部治疗可能会改善KID综合征的皮肤状况,避免全身使用维甲酸治疗可能带来的危害。

相似文献

1
KID syndrome.儿童鱼鳞病样红皮病综合征
Dermatol Online J. 2007 Oct 13;13(4):11.
2
Treatment of keratitis-ichthyosis- deafness (KID) syndrome in children: a case report and review of the literature.儿童角膜炎-鱼鳞病-耳聋(KID)综合征的治疗:一例病例报告及文献综述
Dermatol Ther. 2015 Mar-Apr;28(2):89-93. doi: 10.1111/dth.12192. Epub 2014 Dec 29.
3
[Successful topical cyclosporin A in the therapy of progressive vascularising keratitis in keratitis-ichthyosis-deafness (KID) syndrome (Senter syndrome)].[局部应用环孢素A成功治疗角膜炎-鱼鳞病-耳聋(KID)综合征(森特综合征)中的进行性血管化角膜炎]
Klin Monbl Augenheilkd. 2002 May;219(5):383-6. doi: 10.1055/s-2002-32629.
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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.
5
Marked hyperkeratosis of the soles in keratitis-ichthyosis-deafness syndrome: treatment with hydrocolloid dressing.
Cutis. 2003 Sep;72(3):229-30.
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Severe ichthyosis-related disorders in children: response to acitretin.儿童严重鱼鳞病相关疾病:对阿维A的反应
J Dermatolog Treat. 2007;18(2):118-22. doi: 10.1080/09546630601156348.
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Auditory manifestations of Keratitis-Ichthyosis-Deafness (KID) syndrome.角膜炎-鱼鳞病-耳聋(KID)综合征的听觉表现。
Laryngoscope. 2002 Feb;112(2):272-80. doi: 10.1097/00005537-200202000-00014.
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Diffuse hyperkeratosis in a deaf and blind 48-year-old woman--quiz case. Diagnosis: keratitis-ichthyosis-deafness (KID) syndrome with secondary dermatophytosis.
Arch Dermatol. 2012 Oct;148(10):1199-200. doi: 10.1001/archderm.148.10.1199-c.
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What syndrome is this? KID syndrome (keratitis, ichthyosis, deafness).
Pediatr Dermatol. 2006 Jan-Feb;23(1):81-3. doi: 10.1111/j.1525-1470.2006.00178.x.
10
[Keratitis-ichthyosis-deafness (KID) syndrome: an observation in a child in sub-Saharan Africa].[角膜炎-鱼鳞病-耳聋(KID)综合征:撒哈拉以南非洲一名儿童的病例观察]
Ann Dermatol Venereol. 2011 May;138(5):453-5. doi: 10.1016/j.annder.2011.02.006. Epub 2011 Mar 31.

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Connexin hemichannels influence genetically determined inflammatory and hyperproliferative skin diseases.
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Dental Treatments under the General Anesthesia in a Child with Keratitis, Ichthyosis, and Deafness Syndrome.在一名患有角膜炎、鱼鳞病和耳聋综合征的儿童中进行全身麻醉下的牙科治疗。
Case Rep Dent. 2013;2013:618468. doi: 10.1155/2013/618468. Epub 2013 Sep 18.
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Imaging Keratitis-Icthyosis-Deafness (KID) syndrome with FDG-PET (F18-fluorodeoxiglucose-Positron Emission Tomography).使用氟代脱氧葡萄糖正电子发射断层扫描(FDG-PET,F18-氟代脱氧葡萄糖-正电子发射断层扫描)对角膜鱼鳞病耳聋(KID)综合征进行成像。
J Radiol Case Rep. 2010;4(7):6-11. doi: 10.3941/jrcr.v4i7.381. Epub 2010 Jul 1.
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The Cx26-G45E mutation displays increased hemichannel activity in a mouse model of the lethal form of keratitis-ichthyosis-deafness syndrome.Cx26-G45E 突变在致死性角膜-鱼鳞癣-耳聋综合征的小鼠模型中显示增强的半通道活性。
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