Report of a child with sporadic familial progressive hyper- and hypopigmentation caused by a novel KITLG mutation
Br J Dermatol
.
2016 Dec;175(6):1369-1371.
doi: 10.1111/bjd.14694.
Epub 2016 Sep 27.
Authors
J Zhang
1
,
R Cheng
1
,
J Liang
1
,
C Ni
1
,
M Li
1
,
Z Yao
1
Affiliation
1
Department of Dermatology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai, 200092, China.
PMID:
27106731
DOI:
10.1111/bjd.14694
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Child, Preschool
Humans
Hyperpigmentation / genetics*
Hyperpigmentation / pathology
Hypopigmentation / genetics*
Hypopigmentation / pathology
Male
Mutation, Missense / genetics*
Stem Cell Factor / genetics*
Substances
Stem Cell Factor