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Progeria
oleh: Mohamed Riyaz S, Jayachandran S
Format: | Article |
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Diterbitkan: | Wolters Kluwer Medknow Publications 2009-01-01 |
Deskripsi
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.