Franceschetti–Klein syndrome (also known as "mandibulofacial dysostosis")[1] is a syndrome that includes palpebral antimongoloid fissures, hypoplasia of the facial bones, macrostomia, vaulted palate, malformations of both the external and internal ear, buccal-auricular fistula, abnormal development of the neck with stretching of the cheeks, accessory facial fissures, and skeletal deformities.

[2]: 577 It is sometimes equated with Treacher Collins syndrome.

[3]

This Genodermatoses article is a stub.

You can help Wikipedia by expanding it.