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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Bibliographische Detailangaben
Veröffentlicht in:Case Rep Radiol
Hauptverfasser: Nazir, Haji Mohammed, Ramesh Baabhu, Akshiitha, Muralidharan, Yuvaraj, Cheppala Rajan, Seena
Format: Artigo
Sprache:Inglês
Veröffentlicht: Hindawi 2017
Schlagworte:
Case Report
Online Zugang: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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