Svensk definition
Ärftlig rubbning bestående av multipla basalcellskarcinom, odontogena keratocystor och multipla skeletala defekter. Autosomal ärftlighetsgång.
Ärftlig rubbning bestående av multipla basalcellskarcinom, odontogena keratocystor och multipla skeletala defekter. Autosomal ärftlighetsgång.
Hereditary disorder consisting of multiple basal cell carcinomas, odontogenic keratocysts, and multiple skeletal defects, e.g., frontal and temporoparietal bossing, bifurcated and splayed ribs, kyphoscoliosis, fusion of vertebrae, and cervicothoracic spina bifida. Genetic transmission is autosomal dominant.
Gorlins syndrom
Gorlin Syndrome — Syndrome, Gorlin — Gorlin-Goltz Syndrome — Gorlin Goltz Syndrome — Syndrome, Gorlin-Goltz — NBCCS — Nevoid Basal Cell Carcinoma Syndrome — Nevus Syndrome, Basal Cell — Fifth Phacomatosis — Fifth Phacomatoses — Multiple Basal Cell Nevi, Odontogenic Keratocysts, and Skeletal Anomalies