Familial scaphocephaly syndrome, McGillivray type

MONDO:0012307

Familial scaphocephaly syndrome, McGillivray type is a rare newly described craniosynostosis syndrome characterized by scaphocephaly, macrocephaly, severe maxillary retrusion, and mild intellectual disability.

Also known as: scaphocephaly-macrocephaly-maxillary retrusion-intellectual disability syndrome, scaphocephaly, maxillary retrusion, and intellectual disability, scaphocephaly, maxillary retrusion, and mental retardation

1 clinical trial for this condition and its sub-types, 0 tagged with Familial scaphocephaly syndrome, McGillivray type itself.

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Including sub-types (1) Tagged with Familial scaphocephaly syndrome, McGillivray type (0)

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