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| Title: | Three new families with arterial tortuosity syndrome. |
| Author(s): | Wessels, M.W. Catsman-Berrevoets, C.E. Mancini, G.M. Breuning, M.H. Hoogeboom, J.J. Stroink, H. Frohn-Mulder, I.M. Coucke, P.J. Paepe, A.D. Niermeijer, M.F. (067934250) Willems, P.J. |
| Publication year: | 2004 |
| Document type: | Article / Letter to editor |
| Journal: | American Journal of Medical Genetics Part A |
| ISSN: | 1552-4825 |
| Volume: | vol. 131A |
| Issue: | iss. 2 |
| Start page: | p. 134 |
| End page: | p. 143 |
| Abstract: | Arterial tortuosity syndrome (ATS) is a rare condition with autosomal recessive inheritance characterized by connective tissue abnormalities. The most specific clinical findings are cardiovascular anomalies including tortuosity, lengthening, aneurysm, and stenosis formation of major arteries. Also ventricular hypertrophy is frequently present. Other anomalies are skin hyperextensibility and cutis laxa, joint laxity or contractures of the joints, and inguinal herniae. Histology shows disruption of elastic fibers of the media. These features suggest that ATS is a connective tissue disorder. A biochemical or molecular defect has not yet been identified. We describe here nine additional ATS patients from three consanguineous Moroccan families and review a total of 35 patients with this uncommon condition. |
| Subject: | UMCN 5.1: Genetic defects of metabolism |
| Organization: | UMCN Extern Human Genetics |
| Appears in Collections: | Academic bibliography
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Please use this identifier to cite or link to this item:
http://hdl.handle.net/2066/59229
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