KBG syndrome (Q94173): Difference between revisions
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15 August 2026
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Latest revision as of 09:18, 16 August 2026
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. |
Statements
CID11:ID_465550090
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dki-india-ID_465550090
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Concluído
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15 August 2026
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