KBG syndrome

KBG syndrome is a rare condition characterized by a typical facial dysmorphism, macrodontia of the upper central incisors, skeletal (mainly costovertebral) anomalies and developmental delay.

Also known as: KBG syndrome, short stature-facial and skeletal anomalies-intellectual disability-macrodontia syndrome, KBGS, macrodontia, intellectual disability, characteristic facies, short stature, and skeletal anomalies, macrodontia, mental retardation, characteristic facies, short stature, and skeletal anomalies, short stature, characteristic facies, macrodontia, intellectual disability, and skeletal anomalies, short stature, characteristic facies, macrodontia, mental retardation, and skeletal anomalies

2 clinical trials for this condition and its sub-types, 2 tagged with KBG syndrome itself.