Familial scaphocephaly syndrome, McGillivray type (Q93983)
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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 |
||
| 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. |
Statements
CID11:ID_512057922
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dki-india-ID_512057922
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Concluído
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15 August 2026
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