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Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy.

作者信息

Al-Hamdi Khalil I, Ismael Dooha Khaleel, Qais Saadoon Anwar

机构信息

Department of Medicine, Basra Medical College, Basra, Iraq.

Division of Dermatology, Al-Sadr Teaching Hospital, Basra, Iraq.

出版信息

JAAD Case Rep. 2019 Apr 5;5(4):379-382. doi: 10.1016/j.jdcr.2019.02.014. eCollection 2019 Apr.

DOI:10.1016/j.jdcr.2019.02.014
PMID:31008174
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6453837/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6382/6453837/88a676d233d0/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6382/6453837/24fe3345bc3c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6382/6453837/bdecbeedf8ef/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6382/6453837/c401522895da/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6382/6453837/88a676d233d0/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6382/6453837/24fe3345bc3c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6382/6453837/bdecbeedf8ef/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6382/6453837/c401522895da/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6382/6453837/88a676d233d0/gr4.jpg

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本文引用的文献

1
Clinical and Genetic Review of Hereditary Acral Reticulate Pigmentary Disorders.遗传性肢端网状色素沉着症的临床与遗传学综述
Dermatol Res Pract. 2017;2017:3518568. doi: 10.1155/2017/3518568. Epub 2017 Oct 23.
2
Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder.网状色素性皮病:一种罕见的网状色素沉着性疾病。
Indian Dermatol Online J. 2013 Jan;4(1):40-2. doi: 10.4103/2229-5178.105470.
3
A case of dermatopathia pigmentosa reticularis with wiry scalp hair and digital fibromatosis resulting from a recurrent KRT14 mutation.
一例因KRT14基因反复突变导致的网状色素沉着性皮病伴头皮毛发粗硬及指(趾)纤维瘤病
Clin Exp Dermatol. 2009 Apr;34(3):340-3. doi: 10.1111/j.1365-2230.2008.02950.x. Epub 2008 Nov 24.
4
[Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis. Two allelic ectodermal dysplasias related to mutations of dominant gene coding for keratin 14].[内格利-弗朗切斯科蒂-雅达松综合征与网状色素沉着性皮病。两种与编码角蛋白14的显性基因突变相关的等位基因外胚层发育异常]
Ann Dermatol Venereol. 2007 Jun-Jul;134(6-7):595. doi: 10.1016/s0151-9638(07)89283-0.
5
Reticulate hyperpigmentation.网状色素沉着。
Semin Cutan Med Surg. 1997 Mar;16(1):72-80. doi: 10.1016/s1085-5629(97)80038-7.
6
Dermatopathia pigmentosa reticularis.
Arch Dermatol. 1990 Jul;126(7):935-9.
7
Dermatopathia pigmentosa reticularis: a report of a family demonstrating autosomal dominant inheritance.网状色素性皮病:一个显示常染色体显性遗传的家系报告。
J Am Acad Dermatol. 1992 Feb;26(2 Pt 2):298-301. doi: 10.1016/0190-9622(92)70039-i.