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
A case of familial progressive hyperpigmentation with or without hypopigmentation presenting with hypopigmented striae along the lines of Blaschko.
Hida T, Idogawa M, Ishikawa A, Okura M, Sasaki S, Tokino T, Uhara H.