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Franceschetti–Klein syndrome

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(Redirected from Mandibulofacial dysostosis)
Franceschetti–Klein syndrome
Other namesMandibulofacial dysostosis
This condition is inherited in an autosomal dominant manner.
SpecialtyMedical genetics
Franceschetti–Klein syndrome Medical condition

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]

See also

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References

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  1. ^ FRANCESCHETTI A, KLEIN D (1949). "The mandibulofacial dysostosis; a new hereditary syndrome". Acta Ophthalmol (Copenh). 27 (2): 143–224. PMID 18142195.
  2. ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0-7216-2921-0.
  3. ^ Teber OA, Gillessen-Kaesbach G, Fischer S, et al. (November 2004). "Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation". Eur. J. Hum. Genet. 12 (11): 879–90. doi:10.1038/sj.ejhg.5201260. PMID 15340364.
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