Familial progressive hyperpigmentation and hypopigmentation withoutKITLGmutation-Reference-Cited by-同舟云学术

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Familial progressive hyperpigmentation and hypopigmentation withoutKITLGmutation

Published:2016-10-19 Issue:8 Volume:41 Page:927-929
ISSN:0307-6938
Container-title:Clinical and Experimental Dermatology
language:en
Short-container-title:Clin Exp Dermatol

Author:

Zeng L.¹²,Zheng X. D.¹²,Liu L. H.³,Fu L. Y.¹²,Zuo X. B.¹²,Chen G.¹²,Wang P. G.¹²,Yang S.¹²,Zhang X. J.¹²

Affiliation:

1. Department of Dermatology; No. 1 Affiliated Hospital; Anhui Medical University; Hefei Anhui China

2. State Key Laboratory Incubation Base of Dermatology; Ministry of National Science and Technology; Hefei Anhui China

3. Department of Dermatology; Affiliated Hospital of Jiujiang University; Jiujiang Jiangxi China

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ced.12923/fullpdf

Reference5 articles.

1. Hereditary congenital hypopigmented and hyperpigmented macules;Westerhof;Arch Dermatol,1978

2. KITLG mutations cause familial progressive hyper- and hypopigmentation;Amyere;J Invest Dermatol,2011

3. Progressive hyperpigmentation and generalized lentiginosis without associated systemic symptoms: a rare hereditary pigmentation disorder in south-east Germany;Zanardo;Acta Derm Venereol,2004

4. Familial hyper- and hypopigmentation with age-related pattern change;Hoo;Am J Med Genet A,2005

5. Familial progressive hyper- and hypopigmentation and malignancy in two families with new mutations in KITLG;Cuell;Clin Exp Dermatol,2015

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Identification of a novel mutation in the KITLG gene in a Chinese family with familial progressive hyper- and hypopigmentation;BMC Medical Genomics;2021-01-06

2. Café noir spots: a feature of familial progressive hyper‐ and hypopigmentation;Journal of the European Academy of Dermatology and Venereology;2019-10-24

3. Pigmentary Disorder;Atlas of Skin Disorders;2018

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