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.WoSScopu
Copyright © 2014 Yeliz Bilir et al.This is an open access article distributed under theCreative Comm...
Gorlin-Goltz syndrome or basal cell nevus syndrome is an autosomal dominant syndrome characterized b...
Mirror movements are involuntary movements that occur in homologous contralateral muscles on volunta...
Gorlin syndrome is an autosomal dominant inherited condition that exhibits high penetrance and varia...
Gorlin syndrome, also known as nevoid basal cell carcinoma syndrome, is a rare autosomal dominant di...
The Gorlin-Goltz syndrome, nevoid basal cell carcinoma syndrome, or basal cell nevus syndrome is an ...
PubMedID: 25818966Gorlin-Goltz syndrome is an uncommon disorder transmitted through autosomal domina...
AbstractINTRODUCTIONGorlin syndrome (GS), also known as nevoid basal cell carcinoma syndrome (NBCCS)...
Gorlin syndrome is an autosomal dominant disorder linked to PTCH1 mutation, identified by a collecti...
Gorlin-Goltz syndrome also known as nevoid basal cell carcinoma syndrome (NBCCS) is an infrequent mu...
Gorlin syndrome or basal cell nevus syndrome (BCNS) is a rare autosomal dominant disorder. The condi...
Background: Moebius syndrome is a rare disorder with minimum clinical criteria of congenital facial ...
Dystroglycanopathies are a heterogeneous group of muscular dystrophies often associated with variabl...
Gorlin syndrome is a rare autosomal dominant disorder exhibiting high penetrance and variable expres...
The Gorlin-Goltz syndrome is an infrequent multisystemic disease, which is inherited in an autosomal...
Copyright © 2014 Yeliz Bilir et al.This is an open access article distributed under theCreative Comm...
Gorlin-Goltz syndrome or basal cell nevus syndrome is an autosomal dominant syndrome characterized b...
Mirror movements are involuntary movements that occur in homologous contralateral muscles on volunta...
Gorlin syndrome is an autosomal dominant inherited condition that exhibits high penetrance and varia...
Gorlin syndrome, also known as nevoid basal cell carcinoma syndrome, is a rare autosomal dominant di...
The Gorlin-Goltz syndrome, nevoid basal cell carcinoma syndrome, or basal cell nevus syndrome is an ...
PubMedID: 25818966Gorlin-Goltz syndrome is an uncommon disorder transmitted through autosomal domina...
AbstractINTRODUCTIONGorlin syndrome (GS), also known as nevoid basal cell carcinoma syndrome (NBCCS)...
Gorlin syndrome is an autosomal dominant disorder linked to PTCH1 mutation, identified by a collecti...
Gorlin-Goltz syndrome also known as nevoid basal cell carcinoma syndrome (NBCCS) is an infrequent mu...
Gorlin syndrome or basal cell nevus syndrome (BCNS) is a rare autosomal dominant disorder. The condi...
Background: Moebius syndrome is a rare disorder with minimum clinical criteria of congenital facial ...
Dystroglycanopathies are a heterogeneous group of muscular dystrophies often associated with variabl...
Gorlin syndrome is a rare autosomal dominant disorder exhibiting high penetrance and variable expres...
The Gorlin-Goltz syndrome is an infrequent multisystemic disease, which is inherited in an autosomal...
Copyright © 2014 Yeliz Bilir et al.This is an open access article distributed under theCreative Comm...
Gorlin-Goltz syndrome or basal cell nevus syndrome is an autosomal dominant syndrome characterized b...
Mirror movements are involuntary movements that occur in homologous contralateral muscles on volunta...