Hutchinson-Gilford progeria syndrome with severe calcific aortic valve stenosis

Hutchinson-Gilford progeria syndrome (HGPS) is a rare premature aging syndrome that results from mutation in the Laminin A gene. This case report of a 12-year-old girl with HGPS is presented for the rarity of the syndrome and the classical clinical features that were observed in the patient. All pat...

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Main Authors: Natesh B Hanumanthappa (Author), Ganigara Madhusudan (Author), Jayaranganath Mahimarangaiah (Author), Cholenahally N Manjunath (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2011-01-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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