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Resolution of pseudoainhum with acitretin therapy in a patient with palmoplantar keratoderma and congenital alopecia.

作者信息

Richey Patricia M, Stone Mary S

机构信息

Department of Dermatology, University of Iowa Hospitals and Clinics, Iowa City, Iowa.

Department of Dermatology and Pathology, University of Iowa Hospitals and Clinics, Iowa City, Iowa.

出版信息

JAAD Case Rep. 2019 Feb 12;5(3):219-221. doi: 10.1016/j.jdcr.2018.12.004. eCollection 2019 Mar.

DOI:10.1016/j.jdcr.2018.12.004
PMID:30809564
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6374960/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9689/6374960/fc41b1248e27/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9689/6374960/56f08b8c1927/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9689/6374960/0c550371ee58/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9689/6374960/bf8a99d6611c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9689/6374960/fc41b1248e27/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9689/6374960/56f08b8c1927/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9689/6374960/0c550371ee58/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9689/6374960/bf8a99d6611c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9689/6374960/fc41b1248e27/gr4.jpg

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本文引用的文献

1
Reversal of pseudo-ainhum with acitretin in Camisa's syndrome.阿维A治疗卡米萨综合征假性自发性断指的疗效观察
Indian J Dermatol Venereol Leprol. 2014 Nov-Dec;80(6):572-4. doi: 10.4103/0378-6323.144220.
2
Palmoplantar keratoderma, pseudo-ainhum, and universal atrichia: A new patient and review of the palmoplantar keratoderma-congenital alopecia syndrome.掌跖角化病、假性并指畸形和全身性无毛发：一位新患者及掌跖角化病-先天性秃发综合征的回顾。
Am J Med Genet A. 2010 Aug;152A(8):2043-7. doi: 10.1002/ajmg.a.33490.
3
Vohwinkel Syndrome secondary to missense mutation D66H in GJB2 gene (connexin 26) can include epileptic manifestations.
Open Access Maced J Med Sci. 2019 Sep 10;7(18):3013-3014. doi: 10.3889/oamjms.2019.681. eCollection 2019 Sep 30.
Vohwinkel 综合征继发于 GJB2 基因（连接蛋白 26）错义突变 D66H，可包括癫痫表现。
Seizure. 2010 Mar;19(2):129-31. doi: 10.1016/j.seizure.2009.11.009. Epub 2010 Jan 19.
4
Alopecia congenita: the incomplete dominant form of inheritance with varying expressivity.先天性脱发：具有不同表现度的不完全显性遗传形式。
Acta Genet Stat Med. 1959;9:127-32.
5
Ichthyosis follicularis with atrichia and photophobia (IFAP) syndrome in two unrelated female patients.两名无血缘关系女性患者的毛囊性鱼鳞病伴毛发缺失和畏光（IFAP）综合征
J Am Acad Dermatol. 2002 May;46(5 Suppl):S156-8. doi: 10.1067/mjd.2002.112930.
6
Possible second case of tricho-oculo-dermo-vertebral (Alves) syndrome.毛发-眼-皮肤-脊柱（阿尔维斯）综合征可能的第二例病例。
Am J Med Genet. 1993 May 15;46(3):313-5. doi: 10.1002/ajmg.1320460315.
7
Keratoderma, hypotrichosis and leukonychia totalis: a new syndrome?掌跖角化症、毛发稀少和全白甲：一种新综合征？
Br J Dermatol. 1995 Oct;133(4):636-8. doi: 10.1111/j.1365-2133.1995.tb02720.x.
8
Etretinate: management of keratoma hereditaria mutilans in four family members.依曲替酯：四名家庭成员遗传性残毁性角皮瘤的治疗
J Am Acad Dermatol. 1985 Jul;13(1):43-9. doi: 10.1016/s0190-9622(85)70141-7.
9
Cataracts, alopecia, and sclerodactyly: a previously apparently undescribed ectodermal dysplasia syndrome on the island of Rodrigues.
Am J Med Genet. 1989 Apr;32(4):500-3. doi: 10.1002/ajmg.1320320415.
10
Keratoma hereditaria mutilans (Vohwinkel's disease) with congenital alopecia universalis (atrichia congenita).遗传性残毁性角皮瘤（沃温克尔病）伴先天性全秃（先天性无毛症）。
J Dermatol. 1989 Jun;16(3):231-6. doi: 10.1111/j.1346-8138.1989.tb01255.x.