Familial scaphocephaly syndrome, McGillivray type (Q93983): Difference between revisions
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Revision as of 09:05, 16 August 2026
Familial scaphocephaly syndrome, McGillivray type is a rare craniosynostosis syndrome characterised by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_512057922 |
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| English | Familial scaphocephaly syndrome, McGillivray type |
Familial scaphocephaly syndrome, McGillivray type is a rare craniosynostosis syndrome characterised by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability. |
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CID11:ID_512057922
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dki-india-ID_512057922
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