Apert's syndrome: A rare craniofacial disorder

• Hoofdauteurs: Prajakta C Khelkar (Auteur), Aaditi N Kadam (Auteur), Freny R Karjodkar (Auteur), Kaustubh P Sansare (Auteur)
• Formaat: Boek
• Gepubliceerd in: Wolters Kluwer Medknow Publications, 2020-01-01T00:00:00Z.
• Onderwerpen: article
• Online toegang: Connect to this object online.

Apert's syndrome (AS) which is a rare congenital disorder is a form of acrocephalosyndactyly. This syndrome is characterized by craniosynostosis, midface hypoplasia, and syndactyly of hands and feet. We report a case of 13-year-old boy in India presenting features of AS such as exophthalmos, hy...