MAMC Journal of Medical Sciences

CASE REPORT
Year
: 2018  |  Volume : 4  |  Issue : 2  |  Page : 96--99

Clinical and Radiological Evaluation of Franceschetti Syndrome (Treacher Collins Syndrome): A Rare Case Report


Shalu Rai, Kuber Tyagi, Deepankar Misra, Mansi Khatri, Prerna Jain 
 Department of Oral Medicine & Radiology, Institute of Dental Studies and Technologies, Modinagar, Uttar Pradesh, India

Correspondence Address:
Dr. Shalu Rai
Department of Oral Medicine & Radiology, Institute of Dental Studies and Technologies, Kadrabad, Modinagar 201201, Uttar Pradesh
India

Franceschetti Syndrome is an autosomal dominant disorder of craniofacial development with variable expressivity. It affects structures which are derivatives of the first and second brachial arches. It has a characteristic facial appearance as a result of hypoplasia of facial bones, accompanied by ear, eye and nose abnormalities and positive coloboma sign. This article describes clinical and radiographic features of this syndrome in a 22 year old male who reported to our department with the complaint of pain in his left upper back and right lower back tooth region showing incomplete clinical form of Franceschetti syndrome. Also pathogenesis, diagnosis, prevention, management are discussed.


How to cite this article:
Rai S, Tyagi K, Misra D, Khatri M, Jain P. Clinical and Radiological Evaluation of Franceschetti Syndrome (Treacher Collins Syndrome): A Rare Case Report.MAMC J Med Sci 2018;4:96-99


How to cite this URL:
Rai S, Tyagi K, Misra D, Khatri M, Jain P. Clinical and Radiological Evaluation of Franceschetti Syndrome (Treacher Collins Syndrome): A Rare Case Report. MAMC J Med Sci [serial online] 2018 [cited 2020 Feb 18 ];4:96-99
Available from: http://www.mamcjms.in/article.asp?issn=2394-7438;year=2018;volume=4;issue=2;spage=96;epage=99;aulast=Rai;type=0