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Article Dans Anglais | IMSEAR | ID: sea-139786

Résumé

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.


Sujets)
Adulte , Anodontie/diagnostic , Sutures crâniennes/malformations , Malformations crâniofaciales/diagnostic , Diagnostic différentiel , Os frontal/malformations , Humains , Mâle , Mandibule/malformations , Condyle mandibulaire/malformations , Nez/malformations , Os pariétal/malformations , Progeria/diagnostic
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