Variants
Sign InSign Up

Familial scaphocephaly syndrome, McGillivray type

Your Results

Sign In

Description

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.

ORDO

  • Mode of Inheritance

    VARIANTS

    10

    SEE THE VARIANTS →

    Genes

    External Links

    • OMIM

      609579

    • Orphanet

      168624

    • HPO
    • Medgen

      C1865070

    © 2024 Biocodify. All rights reserved.

    TwitterTwitter

    Product

    HomePricingDashboard

    Stay up to date

    The latest news and updates from Biocodify, sent to your inbox.