KBG syndrome (Q94173)
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KBG syndrome is a rare malformation syndrome characterised by a typical facial dysmorphism, macrodontia of the upper central incisors, skeletal (mainly costovertebral) anomalies and developmental delay.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_465550090 |
||
| English | KBG syndrome |
KBG syndrome is a rare malformation syndrome characterised by a typical facial dysmorphism, macrodontia of the upper central incisors, skeletal (mainly costovertebral) anomalies and developmental delay. |
