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Concept information

disease > genetic disease > hereditary disease > mandibulofacial dysostosis
disease > stomatology > mandibulofacial dysostosis
disease > stomatology > maxillary disease > mandibulofacial dysostosis
disease > stomatology > dysmorphic facies > mandibulofacial dysostosis
... > disease > congenital disease > malformation > dysmorphia > dysmorphic facies > mandibulofacial dysostosis
disease > congenital disease > malformation > dysostosis > mandibulofacial dysostosis
disease > diseases of the osteoarticular system > dysostosis > mandibulofacial dysostosis

Terme préférentiel

mandibulofacial dysostosis  

Définition(s)

  • 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. (Wikipedia)
  • Treacher Collins syndrome (TCS) is a genetic disorder characterized by deformities of the ears, eyes, cheekbones, and chin. (Wikipedia)

Concept(s) générique(s)

Concept(s) spécifique(s)

Synonyme(s)

  • Treacher-Collins syndrome

Traductions

URI

http://data.loterre.fr/ark:/67375/VH8-KSS0VVWV-B

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