Novel KIT Mutation Presenting As Marked Lentiginosis
Overview
Overview
Journal
Pediatr Dermatol
Publisher
Wiley
Specialties
Dermatology
Pediatrics
Pediatrics
Date
2019 Sep 10
PMID
31497890
Citations
2
Authors
Affiliations
Affiliations
Soon will be listed here.
Abstract
Although lentigines are usually benign, they can be associated with a number of genetic syndromes in which neoplasms and other multi-system pathological processes occur. Here, we report the case of a 6-year-old girl who presented with atypical lentiginosis and hyperpigmentation caused by a de novo genetic variant in the KIT gene.
Citing Articles
Ge Q, Liu Y, Yang F, Sun G, Guo J, Sun S Int J Mol Sci. 2023; 24(1).
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Yang L, Liu Y, Wang T Front Med (Lausanne). 2022; 9:847382.
PMID: 35692550 PMC: 9174787. DOI: 10.3389/fmed.2022.847382.