Familial scaphocephaly syndrome, McGillivray type (Q93983): Difference between revisions
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Síndrome da escafocefalia familiar, tipo McGillivray, é uma síndrome de craniossinostose rara caracterizada por escafocefalia, macrocefalia, retrusão maxilar grave e incapacidade intelectual leve. | |||
| description / en | description / en | ||
Familial scaphocephaly syndrome, McGillivray type is a rare craniosynostosis syndrome characterised by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability. | |||
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 |
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| 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. |
