Familial progressive hyperpigmentation: a case report.
Yadav M, Ghonasgi S, Shah R, Meghana SM.
Case Rep Dent. 2012;2012:840167. doi: 10.1155/2012/840167. Epub 2012 Apr 18.
PMID:22577587
A novel KITLG mutation causes familial progressive hyperpigmentation and hypopigmentation with multiple cafe-au-lait macules.
Huang X, Niu G, Lin Z, Wang H.
Indian J Dermatol Venereol Leprol. 2024 Jul 1:1-3. doi: 10.25259/IJDVL_1246_2023. Online ahead of print.
PMID:39152874
Familial Progressive Hyperpigmentation, Cutaneous Mastocytosis, and Gastrointestinal Stromal Tumor as Clinical Manifestations of Mutations in the c-KIT Receptor Gene.
Piqueres-Zubiaurre T, Martínez de Lagrán Z, González-Pérez R, Urtaran-Ibarzabal A, Perez de Nanclares G.
Pediatr Dermatol. 2017 Jan;34(1):84-89. doi: 10.1111/pde.13040. Epub 2016 Dec 16.
PMID:27981619
Novel mutation in the KITLG gene in familial progressive hyperpigmentation with or without hypopigmentation.
Kato M, Yagami A, Tsukamoto T, Shinkai Y, Kato T, Kurahashi H.
J Dermatol. 2020 Jun;47(6):669-672. doi: 10.1111/1346-8138.15313. Epub 2020 Mar 18.
PMID:32189379
Familial progressive hyperpigmentation: a family study in China.