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Novel KIT mutation presenting as marked lentiginosis

Authors :
Luis A. Pérez-Jurado
Marcos López-Sánchez
Alain K Tran
Annette Pearce
Christopher Barnett
Source :
Pediatric Dermatology. 36:922-925
Publication Year :
2019
Publisher :
Wiley, 2019.

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.

Details

ISSN :
15251470 and 07368046
Volume :
36
Database :
OpenAIRE
Journal :
Pediatric Dermatology
Accession number :
edsair.doi...........d007929cea5bdeb9032f61f6a50551e5