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Role of Trichoscopy in diagnosing Genotrichosis-A Report of Two Cases.

作者信息

Reyaz Saika, Bhat Yasmeen Jabeen, Ismail Ishrat Binti, Saqib Najam U, Trumboo Taiba

机构信息

Department of Dermatology, Government Medical College, Srinagar, Jammu and Kashmir, India.

出版信息

Indian Dermatol Online J. 2025 Sep 1;16(5):800-802. doi: 10.4103/idoj.idoj_398_24. Epub 2025 May 26.

DOI:10.4103/idoj.idoj_398_24
PMID:40709852
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12419726/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ab/12419726/0739254a1f1d/IDOJ-16-800-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ab/12419726/f0ec4a702dae/IDOJ-16-800-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ab/12419726/4a08bc0e0272/IDOJ-16-800-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ab/12419726/e24e32167bfb/IDOJ-16-800-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ab/12419726/31ba8c1da973/IDOJ-16-800-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ab/12419726/035a1cde7199/IDOJ-16-800-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ab/12419726/0739254a1f1d/IDOJ-16-800-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ab/12419726/f0ec4a702dae/IDOJ-16-800-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ab/12419726/4a08bc0e0272/IDOJ-16-800-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ab/12419726/e24e32167bfb/IDOJ-16-800-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ab/12419726/31ba8c1da973/IDOJ-16-800-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ab/12419726/035a1cde7199/IDOJ-16-800-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ab/12419726/0739254a1f1d/IDOJ-16-800-g006.jpg

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本文引用的文献

1
Pili Torti: A Feature of Numerous Congenital and Acquired Conditions.扭曲发:众多先天性和后天性疾病的一个特征。
J Clin Med. 2021 Aug 30;10(17):3901. doi: 10.3390/jcm10173901.
2
Congenital atrichia with papular lesions.先天性无毛症伴丘疹性皮损。
Dermatol Online J. 2020 Apr 15;26(4):13030/qt5631x9sh.
3
Novel compound heterozygous mutations in BCS1L gene causing Bjornstad syndrome in two siblings.BCS1L基因中的新型复合杂合突变导致两名兄弟姐妹患比约恩斯塔德综合征。
Am J Med Genet A. 2017 May;173(5):1348-1352. doi: 10.1002/ajmg.a.38146. Epub 2017 Mar 21.
4
Atrichia with papular lesions: a report of three novel human hairless gene mutations and a revision of diagnostic criteria.伴有丘疹性损害的无毛症:3个新的人类无毛基因突变报告及诊断标准修订
Acta Derm Venereol. 2008;88(4):346-9. doi: 10.2340/00015555-0466.
5
Atrichia caused by mutations in the vitamin D receptor gene is a phenocopy of generalized atrichia caused by mutations in the hairless gene.维生素D受体基因突变引起的无毛症是无毛基因突变导致的全身性无毛症的表型模拟。
J Invest Dermatol. 2001 Sep;117(3):612-7. doi: 10.1046/j.0022-202x.2001.01438.x.