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Langer-Giedion Syndrome: a Rare Case Report | ||
Journal of Dentistry | ||
مقاله 12، دوره 17، شماره 3، آذر 2016، صفحه 238-241 اصل مقاله (630.87 K) | ||
نوع مقاله: Case Report | ||
نویسندگان | ||
Farhin Ali Katge* 1؛ Bhavesh Dahyabhai Rusawat1؛ Pooja Ravindra Shivasharan2؛ Devendra Pandurang Patil2 | ||
1Dept. of Pedodontics & Preventive Dentistry, Terna Dental College, Navi Mumbai, Maharashtra, India. | ||
2Postgraduate Student, Dept. of Pedodontics & Preventive Dentistry, Terna Dental College, Navi Mumbai, India. | ||
چکیده | ||
Langer-Giedion syndrome is a very uncommon autosomal dominant genetic disorder caused by the deletion of chromosomal material. It is characterized by multiple bony exostosis, short stature, mental retardation, and typical facial features. The characteristic appearance of individuals includes sparse scalp hair, rounded nose, prominent philtral area and thin upper lip. Some cases with this condition have loose skin in childhood which typically resolves with age. Oral and dental manifestations include micrognathia, retrognathia, hypodontia, and malocclusion based on cephalometric analysis. This report presents a case of Langer-Giedion syndrome in a 10-year-old child. Keywords ● Trichorhinophalangeal Syndrome type 2 ● Exostosis ● Hypodontia ● Langer-Giedion Syndrome | ||
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