KBG syndrome
Abstract Clinical Description KBG syndrome is characterized by macrodontia of upper central incisors, distinctive craniofacial features such as triangular face, prominent nasal bridge, thin upper lip and synophrys; skeletal findings including short stature, delayed bone age, and costovertebral anoma...
Main Authors: | Dayna Morel Swols, Joseph Foster, Mustafa Tekin |
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Format: | Article |
Language: | English |
Published: |
BMC
2017-12-01
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Series: | Orphanet Journal of Rare Diseases |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s13023-017-0736-8 |
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