Open AccessProgeria
Author(s) -
Jayachandran Sadaksharam,
Mohamed Abdulcader Riyaz
Publication year - 2009
Publication title -
indian journal of dental research
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.277
H-Index - 43
eISSN - 1998-3603
pISSN - 0970-9290
DOI - 10.4103/0970-9290.59442
Subject(s) - progeria , medicine , premature aging , differential diagnosis , stroke (engine) , dermatology , pediatrics , pathology , genetics , biology , physiology , gene , mechanical engineering , engineering
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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