Мы используем файлы cookie.
Продолжая использовать сайт, вы даете свое согласие на работу с этими файлами.
Franceschetti–Klein syndrome
Другие языки:

Franceschetti–Klein syndrome

Подписчиков: 0, рейтинг: 0
Franceschetti–Klein syndrome
Other names Mandibulofacial dysostosis
Autosomal dominant - en.svg
This condition is inherited in an autosomal dominant manner.

Franceschetti–Klein syndrome (also known as "mandibulofacial dysostosis") 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.It is sometimes equated with Treacher Collins syndrome.

See also

External links



Новое сообщение