Progeria.

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dc.contributor.authorRiyaz, S S Mohamed
dc.contributor.authorJayachandran, S
dc.date.accessioned2012-07-24T07:23:20Z
dc.date.available2012-07-24T07:23:20Z
dc.date.issued2009-10
dc.description.abstractHutchinson 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.en_US
dc.identifier.citationRiyaz S S Mohamed, Jayachandran S. Progeria. Indian Journal of Dental Research. 2009 Oct-Dec; 20(4): 508-510.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/139786
dc.language.isoenen_US
dc.source.urihttps://www.ijdr.in/article.asp?issn=0970-9290;year=2009;volume=20;issue=4;spage=508;epage=510;aulast=Mohameden_US
dc.subjectHutchinson-Gilford progeria syndromeen_US
dc.subjectHGPSen_US
dc.subjectpremature ageingen_US
dc.subject.meshAdult
dc.subject.meshAnodontia --diagnosis
dc.subject.meshCranial Sutures --abnormalities
dc.subject.meshCraniofacial Abnormalities --diagnosis
dc.subject.meshDiagnosis, Differential
dc.subject.meshFrontal Bone --abnormalities
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMandible --abnormalities
dc.subject.meshMandibular Condyle --abnormalities
dc.subject.meshNose --abnormalities
dc.subject.meshParietal Bone --abnormalities
dc.subject.meshProgeria --diagnosis
dc.titleProgeria.en_US
dc.typeArticleen_US
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