Karakurt, CemşitKoçak, GülendamElkıran, ÖzlemCoucke; PJVan Maldergem; L.2017-08-232017-08-232012Karakurt, C. Koçak, G. Elkıran, Ö. Coucke; PJ. Van Maldergem; L. (2012). Arterial tortuosity syndrome case report. Genet Couns. 23(4):477-482.https://hdl.handle.net/11616/7696Arterial tortuosity syndrome (ATS; OMIM 208050) is a rare autosomal recessive condition characterized by dysmorphic features, elongation, tortuosity, and aneurysm of the large and middle sized arteries. We report on a 13-year-old boy who presented with a malformed ascending aorta mimicking coarctation of aorta and a cutis laxa-like facial dysmorphia. Based on angiogram, a diagnosis of ATS was made and subsequently confirmed by a homozygous one base-pair deletion at position g.318 of SLCA10. We stress similarities (facial appearance, inguinal herniae, ..) between ATS and autosomal recessive cutis laxa, both being connective tissue disorders disorganizing the elastin network.eninfo:eu-repo/semantics/embargoedAccessArticle234477482