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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Detalles Bibliográficos
Autores principales: Nazir, Haji Mohammed, Ramesh Baabhu, Akshiitha, Muralidharan, Yuvaraj, Cheppala Rajan, Seena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613360/
https://www.ncbi.nlm.nih.gov/pubmed/29138706
http://dx.doi.org/10.1155/2017/1305360

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613360/
https://www.ncbi.nlm.nih.gov/pubmed/29138706
http://dx.doi.org/10.1155/2017/1305360

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