| Literature DB >> 26917672 |
Erdal Sag1, Rahsan Gocmen2, F Gokcem Yildiz3, Zeynelabidin Ozturk4, Cagri Temucin5, Ozlem Teksam4, Eda Utine6.
Abstract
Congenital mirror movements are rare conditions that define the inability to perform unimanual movements. Gorlin syndrome, also known as nevoid basal cell carcinoma syndrome, is a genetic disorder with multiple nevi predisposing to basal cell carcinoma, odontogenic keratocysts, and skeletal malformations. Herein we report on an adolescent patient with Gorlin syndrome and coexisting congenital mirror movements. To our knowledge, this is the first patient in the literature who has both of these very rare conditions.Entities:
Mesh:
Year: 2016 PMID: 26917672 DOI: 10.1542/peds.2015-1771
Source DB: PubMed Journal: Pediatrics ISSN: 0031-4005 Impact factor: 7.124