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Nevus comedonicus syndrome: A systematic review of the literature

Authors :
Daniele Torchia
Source :
Pediatric Dermatology. 38:359-363
Publication Year :
2021
Publisher :
Wiley, 2021.

Abstract

Nevus comedonicus (NC) syndrome is a condition first identified in 1978. The cause of NC syndrome has been recently proven to be a gain-of-function, mosaic postzygotic mutation of the NEK9 gene. A systematic review of the literature retrieved 43 well-established cases of NC syndrome reported so far. Three morphological variants of NC in NC syndrome emerged: (a) the more common, predominantly comedonal type; (b) "Selhorst type"; and (c) "atrophoderma vermiculatum" type. NC syndrome is mainly associated with ocular, skeletal, and neural abnormalities, most typically ipsilateral congenital cataract and malformations of fingers and toes.

Details

ISSN :
15251470 and 07368046
Volume :
38
Database :
OpenAIRE
Journal :
Pediatric Dermatology
Accession number :
edsair.doi.dedup.....0365086c53e416340da54ab5b90ff28e
Full Text :
https://doi.org/10.1111/pde.14508