Progeria.
Article
Dans Anglais
| IMSEAR
| ID: sea-139786
ABSTRACT
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.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Sujet Principal:
Os pariétal
/
Progeria
/
Humains
/
Mâle
/
Nez
/
Malformations crâniofaciales
/
Adulte
/
Sutures crâniennes
/
Diagnostic différentiel
/
Os frontal
Type d'étude:
Etude diagnostique
langue:
Anglais
Année:
2009
Type:
Article
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