McGillivray syndrome
Familial scaphocephaly syndrome, McGillivray type is a rare newly described craniosynostosis (see this term) syndrome characterized by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability
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McGillivray syndrome
Summary
McGillivray syndrome is a developmental defect during embryogenesis[1].
Key Facts
- McGillivray syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- McGillivray syndrome's instance of is recorded as rare disease[3].
- McGillivray syndrome's instance of is recorded as class of disease[4].
- McGillivray syndrome is a type of scaphocephaly[5].
- McGillivray syndrome is a type of familial scaphocephaly syndrome[6].
- McGillivray syndrome's health specialty is recorded as cardiology[7].
- McGillivray syndrome's genetic association is recorded as FGFR2[8].
- McGillivray syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_168624[9].