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SHORT COMMUNICATION Table of Contents   
Year : 2009  |  Volume : 20  |  Issue : 4  |  Page : 508-510
Progeria


Department of Oral Medicine, Diagnosis and Radiology, Tamil Nadu Government Dental College and Hospital, Chennai, India

Correspondence Address:
S Jayachandran
Department of Oral Medicine, Diagnosis and Radiology, Tamil Nadu Government Dental College and Hospital, Chennai
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0970-9290.59442

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Hutchinson Gilford Progeria Syndrome (HGPS) is a rare, sporadic, autosomal dominant syndrome that involves premature ageing and death at early age due to myocardial infarction or stroke. A 30-year-old male with clinical and radiologic features highly suggestive of HGPS is presented here with description of differential diagnosis, dental considerations and review of literature.


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