KBG syndrome

Disease Export to PDF
Name:
KBG syndrome
Description:
A rare congenital malformation syndrome characterized by a typical facial dysmorphism, macrodontia of the permanent upper central incisors, short stature, skeletal anomalies, developmental delay and behavioral abnormalities.
ORPHAcode:
2332
Synonyms:
Short stature-facial and skeletal anomalies-intellectual disability-macrodontia syndrome
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14