/KBG syndrome

KBG syndrome

Rare Disease

MONDO:0007846

Also Known As

KBG syndromeshort stature-facial and skeletal anomalies-intellectual disability-macrodontia syndromeKBGSmacrodontia, intellectual disability, characteristic facies, short stature, and skeletal anomaliesmacrodontia, mental retardation, characteristic facies, short stature, and skeletal anomaliesshort stature, characteristic facies, macrodontia, intellectual disability, and skeletal anomaliesshort stature, characteristic facies, macrodontia, mental retardation, and skeletal anomalies

Definition

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.