KBG syndrome (Q94173): Difference between revisions
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Síndrome KBG é uma síndrome de malformação rara caracterizada por um dismorfismo facial típico, macrodontia dos incisivos centrais superiores, anomalias esqueléticas (principalmente costovertebrais) e atraso no desenvolvimento. | |||
| description / en | description / en | ||
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. | |||
Revision as of 09:17, 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. |
