Report of a child with sporadic familial progressive hyper- and hypopigmentation caused by a novelKITLGmutation-Reference-Cited by-同舟云学术

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Report of a child with sporadic familial progressive hyper- and hypopigmentation caused by a novelKITLGmutation

Published:2016-09-27 Issue:6 Volume:175 Page:1369-1371
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:Br J Dermatol

Author:

Zhang J.¹,Cheng R.¹,Liang J.¹,Ni C.¹,Li M.¹,Yao Z.¹

Affiliation:

1. Department of Dermatology; Xinhua Hospital; Shanghai Jiaotong University School of Medicine; 1665 Kongjiang Road Shanghai 200092 China

Funder

National Natural Science Foundation of China

Research Fund for the Doctoral Program of Higher Education

Natural Science Foundation of Shanghai

Foundation of Xinhua Hospital affiliated to the Shanghai Jiaotong University School of Medicine

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjd.14694/fullpdf

Reference10 articles.

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

2. The genetic determination of skin pigmentation: KITLG and the KITLG/c-Kit pathway as key players in the onset of human familial pigmentary diseases;Picardo;J Invest Dermatol,2011

3. Molecular characterization of NF1 and neurofibromatosis type 1 genotype-phenotype correlations in a Chinese population;Zhang;Sci Rep,2015

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

5. Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation;Wang;Am J Hum Genet,2009

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1. A case of familial progressive hyperpigmentation with or without hypopigmentation presenting with hypopigmented striae along the lines of Blaschko;The Journal of Dermatology;2024-09-13

2. Value of a café‐au‐lait macules screening clinic: Experience from The Hospital for Sick Children in Toronto;Pediatric Dermatology;2022-02-17

3. Updated Approach to Patients with Multiple Café au Lait Macules;Dermatologic Clinics;2022-01

4. De novo mutation in KITLG gene causes a variant of Familial Progressive Hyper‐ and Hypo‐pigmentation (FPHH);Molecular Genetics & Genomic Medicine;2021-10-30

5. Familial progressive hyper‐ and hypopigmentation caused by a novel mutation in site II of the KITLG gene;The Journal of Dermatology;2021-06-11

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