TREACHER COLLINS SYNDROME - A RARE CONGENITAL DISORDER

Author:

Gupta Richa,Moupachi Surendra Singh,Gupta Shikha,Gupta Saurabh,Gupta Pallavi

Publisher

Akshantala Enterprises Private Limited

Subject

General Medicine

Reference8 articles.

1. 1. A Franceschetti , D Klein. The mandibulo-facial dysostosis. A new hereditary syndrome. Acta Ophthalmologica J Craniofacial Surg 1949 ; 27: 143-224.

2. 2. Edwards SJ, Gladwin AJ, Dixon MJ. The mutational spectrum in Treacher Collins syndrome reveals a predominance of mutations that create a prematuretermination codon. Am J Hum Genet 1997; 60: 515-24.

3. 3. Scriver CR. The metabolic & molecular bases of inherited disease. Am J Pathol 2008; 173: 301-10.

4. 4. Moore KL, Persaud TN. The Developing Human: Clinically Oriented Embryolog.8th ed. Philadelphia, PA: Saunders Elsevier; 2008.

5. Treacher Collins syndrome: current evaluation, treatment, andfuture directions;JC;Cleft Palate Craniofac J,2000

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