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...
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2011-01-01
|
Series: | Annals of Pediatric Cardiology |
Subjects: | |
Online Access: | http://www.annalspc.com/article.asp?issn=0974-2069;year=2011;volume=4;issue=2;spage=204;epage=206;aulast=Hanumanthappa |