Combined aortic and mitral stenosis in mucopolysaccharidosis type I-S (Ullrich-Scheie syndrome).

Détails

ID Serval
serval:BIB_1ED30B5D694B
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Titre
Combined aortic and mitral stenosis in mucopolysaccharidosis type I-S (Ullrich-Scheie syndrome).
Périodique
Heart (british Cardiac Society)
Auteur⸱e⸱s
Fischer T.A., Lehr H.A., Nixdorff U., Meyer J.
ISSN
1355-6037 (Print)
ISSN-L
1355-6037
Statut éditorial
Publié
Date de publication
1999
Volume
81
Numéro
1
Pages
97-99
Langue
anglais
Notes
Publication types: Case Reports ; Journal ArticlePublication Status: ppublish
Résumé
The genetic mucopolysaccharidosis syndromes (MPS) are autosomal recessive inborn errors of metabolism. Heart valve involvement in MPS is not uncommon but only a few case reports of successful cardiac surgery are available. In particular, reports of combined aortic and mitral stenosis associated with MPS type I-S are very rare. Both type I and type VI MPS are associated with significant left sided valvar heart disease that requires surgical valve replacement because of irregular valve thickening, fibrosis, and calcification. A 35 year old man had severe mitral valve stenosis after successful surgical replacement of a stenotic aortic valve. Valvar heart disease was investigated by cardiac ultrasound and left heart catheterisation. Histomorphological characterisation of the affected mitral valve was performed. The case illustrates typically associated clinical features of cardiac and extracardiac abnormalities found in MPS type I-S.
Mots-clé
Adult, Aortic Valve Stenosis/complications, Aortic Valve Stenosis/pathology, Echocardiography, Echocardiography, Doppler, Color, Humans, Male, Mitral Valve, Mitral Valve Stenosis/complications, Mitral Valve Stenosis/pathology, Mucopolysaccharidosis I/complications, Mucopolysaccharidosis I/pathology
Pubmed
Création de la notice
27/11/2011 18:39
Dernière modification de la notice
20/08/2019 12:54
Données d'usage