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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

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/59229

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