Radiological Diagnosis of a Rare Premature Aging Genetic Disorder: Progeria (Hutchinson-Gilford Syndrome)

Hutchinson-Gilford Progeria Syndrome (HGPS) is a rare disease with a combination of short stature, bone abnormalities, premature ageing, and skin changes. Though the physical appearance of these patients is characteristic, there is little emphasis on the characteristic radiological features. In this...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Case Rep Radiol
Asıl Yazarlar: Nazir, Haji Mohammed, Ramesh Baabhu, Akshiitha, Muralidharan, Yuvaraj, Cheppala Rajan, Seena
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Hindawi 2017
Konular:
Case Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5613360/
https://ncbi.nlm.nih.gov/pubmed/29138706
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2017/1305360
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