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Progressive Symmetrical Erythrokeratoderma Associated with Punctate Palmoplantarkeratoderma.

作者信息

Tiwary Anup K, Kumar Piyush

机构信息

Department of Dermatology and Venereology, Government Medical College and Hospital, Haldwani, Nainital, Uttarakhand, India.

Department of Dermatology, Katihar Medical College and hospital, Katihar, Bihar, India.

出版信息

Indian Dermatol Online J. 2019 Mar-Apr;10(2):183-186. doi: 10.4103/idoj.IDOJ_105_18.

DOI:10.4103/idoj.IDOJ_105_18
PMID:30984600
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6434765/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd0/6434765/37722974eb9b/IDOJ-10-183-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd0/6434765/826017ae006d/IDOJ-10-183-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd0/6434765/75e639100c43/IDOJ-10-183-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd0/6434765/37722974eb9b/IDOJ-10-183-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd0/6434765/826017ae006d/IDOJ-10-183-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd0/6434765/75e639100c43/IDOJ-10-183-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd0/6434765/37722974eb9b/IDOJ-10-183-g003.jpg

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引用本文的文献

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本文引用的文献

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Progressive symmetrical erythrokeratoderma on the face: A rare condition and successful treatment with calcipotriol.面部进行性对称性红斑角化病:一种罕见病症及使用卡泊三醇的成功治疗案例
JAAD Case Rep. 2016 Feb 4;2(1):70-1. doi: 10.1016/j.jdcr.2015.11.010. eCollection 2016 Jan.
2
Progressive Symmetric Erythrokeratoderma Having Overlapping Features With Erythrokeratoderma Variabilis and Lesional Hypertrichosis: Is Nomenclature "Erythrokeratoderma Variabilis Progressiva" More Appropriate?具有进行性对称性红斑角化病与可变性红斑角化病重叠特征及皮损多毛症:命名为“进行性可变性红斑角化病”是否更合适?
Indian J Dermatol. 2015 Jul-Aug;60(4):410-1. doi: 10.4103/0019-5154.160499.
3
Progressive symmetric erythrokeratoderma with nephrotic syndrome: Coincidence or new association?
进行性对称性红斑角化症伴肾病综合征:巧合还是新的关联?
Indian Dermatol Online J. 2013 Oct;4(4):347-9. doi: 10.4103/2229-5178.120680.
4
Progressive symmetrical erythrokeratoderma: report of two Chinese families and evaluation for mutations in the loricrin, connexin 30.3 and connexin 31 genes.进行性对称性红斑角化病:两个中国家系报告及loricrin、连接蛋白30.3和连接蛋白31基因的突变评估
Clin Exp Dermatol. 2013 Dec;38(8):925-7. doi: 10.1111/ced.12135. Epub 2013 May 17.
5
Progressive symmetric erythrokeratodermia with delayed intellectual milestones and convulsions.伴有智力发育迟缓及惊厥的进行性对称性红斑角化症。
Indian Dermatol Online J. 2012 Jan;3(1):54-6. doi: 10.4103/2229-5178.93502.
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Evidence for the absence of mutations at GJB3, GJB4 and LOR in progressive symmetrical erythrokeratodermia.在进行性对称性红斑角化症中未发现 GJB3、GJB4 和 LOR 基因突变的证据。
Clin Exp Dermatol. 2011 Jun;36(4):399-405. doi: 10.1111/j.1365-2230.2010.03974.x. Epub 2010 Dec 24.
7
The missense mutation G12D in connexin30.3 can cause both erythrokeratodermia variabilis of Mendes da Costa and progressive symmetric erythrokeratodermia of Gottron.连接蛋白30.3中的错义突变G12D可导致门德斯·达·科斯塔变异性红斑角皮病和戈特龙进行性对称性红斑角皮病。
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8
Identification of a novel locus for progressive symmetric erythrokeratodermia to a 19.02-cM interval at 21q11.2-21q21.2.
J Invest Dermatol. 2006 Sep;126(9):2136-9. doi: 10.1038/sj.jid.5700363. Epub 2006 May 11.