Literature DB >> 1296999

Mandibulofacial dysostosis (Treacher Collins syndrome): a case report.

D L Mittman1, O G Rodman.   

Abstract

Mandibulofacial dysostosis, also known as Treacher Collins syndrome, is a rare congenital anomaly that must be identified in infancy to prevent irrevocable developmental impairment. Information is sparse in the current medical literature concerning this rare syndrome. This article reports a case of Treacher Collins syndrome with the presence of a scarring alopecia and acne keloidalis nuchae, which are possibly coincidental symptoms, but have not been previously described clinically in this malady.

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Year:  1992        PMID: 1296999      PMCID: PMC2571652     

Source DB:  PubMed          Journal:  J Natl Med Assoc        ISSN: 0027-9684            Impact factor:   1.798


  5 in total

1.  An atypical case of Treacher Collins syndrome.

Authors:  C E Lliades
Journal:  Ear Nose Throat J       Date:  1978-11       Impact factor: 1.697

2.  Mandibulo-facial dysostosis. (Treacher-Collins syndrome).

Authors:  L E Fazen; J Elmore; H L Nadler
Journal:  Am J Dis Child       Date:  1967-04

3.  The skeletal anatomy of mandibulofacial dysostosis (Treacher Collins syndrome).

Authors:  J L Marsh; S E Celin; M W Vannier; M Gado
Journal:  Plast Reconstr Surg       Date:  1986-10       Impact factor: 4.730

Review 4.  The surgical treatment of mandibulofacial dysostosis (Berry syndrome; Treacher Collins syndrome; Franceschetti-Zwahlen-Klein syndrome).

Authors:  B O Rogers
Journal:  Clin Plast Surg       Date:  1976-10       Impact factor: 2.017

5.  The ear deformities in mandibulofacial dysostosis (Treacher Collins syndrome).

Authors:  P D Phelps; D Poswillo; G A Lloyd
Journal:  Clin Otolaryngol Allied Sci       Date:  1981-02
  5 in total
  1 in total

1.  Treacher Collins syndrome: a case report.

Authors:  Ravi Prakash Sasankoti Mohan; Sankalp Verma; Neha Agarwal; Udita Singh
Journal:  BMJ Case Rep       Date:  2013-05-24
  1 in total

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