Franceschetti–Klein syndrome

Franceschetti–Klein syndrome
Other names	Mandibulofacial dysostosis
This condition is inherited in an autosomal dominant manner.

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]: 577It is sometimes equated with Treacher Collins syndrome.^[3]

See also

• Dysostosis

References