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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Dades bibliogràfiques
Publicat a:Case Rep Radiol
Autors principals: Nazir, Haji Mohammed, Ramesh Baabhu, Akshiitha, Muralidharan, Yuvaraj, Cheppala Rajan, Seena
Format: Artigo
Idioma:Inglês
Publicat: Hindawi 2017
Matèries:
Case Report
Accés en línia: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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