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Eye Diseases > Eye Abnormalities > Coloboma > Mandibulofacial Dysostosis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Eye Abnormalities > Coloboma > Mandibulofacial Dysostosis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Eye Diseases, Hereditary > Coloboma > Mandibulofacial Dysostosis
Eye Diseases > Eye Diseases, Hereditary > Coloboma > Mandibulofacial Dysostosis
Musculoskeletal Diseases > Musculoskeletal Abnormalities > Craniofacial Abnormalities > Craniofacial Dysostosis > Mandibulofacial Dysostosis
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Musculoskeletal Abnormalities > Craniofacial Abnormalities > Craniofacial Dysostosis > Mandibulofacial Dysostosis
... > Musculoskeletal Diseases > Bone Diseases > Bone Diseases, Developmental > Dysostoses > Craniofacial Dysostosis > Mandibulofacial Dysostosis

Preferred term

Mandibulofacial Dysostosis  

Type

  • Topical Descriptor

Broader concept

Narrower concepts

Entry terms

  • Franceschetti Zwahlen Klein Syndrome
  • Franceschetti-Zwahlen-Klein Syndrome
  • Franceschetti-Zwahlen-Klein Syndromes
  • Syndrome, Franceschetti-Zwahlen-Klein
  • Syndromes, Franceschetti-Zwahlen-Klein
  • Syndromes, Treacher Collins-Franceschetti
  • Syndrome, Treacher Collins
  • Syndrome, Treacher Collins-Franceschetti
  • Treacher Collins Franceschetti Syndrome
  • Treacher Collins-Franceschetti Syndrome
  • Treacher Collins-Franceschetti Syndromes
  • Treacher Collins Syndrome

Scope note

  • A hereditary disorder occurring in two forms: the complete form (Franceschetti's syndrome) is characterized by a slant of the palpebral fissures, COLOBOMA of the lower lid, MICROGNATHIA and hypoplasia of the ZYGOMATIC ARCHES, and CONGENITAL MICROTIA. It is transmitted as an autosomal trait. The incomplete form (Treacher Collins syndrome) is characterized by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (Dorland, 27th ed)

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URI

http://www.yso.fi/onto/mesh/D008342

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