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Novel KIT mutation presenting as marked lentiginosis
- 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.
- Subjects :
- medicine.medical_specialty
Genetic syndromes
business.industry
Kit gene
Genetic variants
Dermatology
Kit mutation
medicine.disease
Hyperpigmentation
030207 dermatology & venereal diseases
03 medical and health sciences
0302 clinical medicine
030220 oncology & carcinogenesis
Pediatrics, Perinatology and Child Health
medicine
Lentiginosis
medicine.symptom
business
Pathological
Subjects
Details
- ISSN :
- 15251470 and 07368046
- Volume :
- 36
- Database :
- OpenAIRE
- Journal :
- Pediatric Dermatology
- Accession number :
- edsair.doi...........d007929cea5bdeb9032f61f6a50551e5