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Abstract
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant vascular dysplasia characterized by telangiectases and arteriovenous malformations. These lesions cause bleeding, particularly in the nose, gastrointestinal tract and brain. HHT has incomplete penetrance, variable expressivity and genetic heterogeneity. De novo mutations associated with the onset of sporadic HHT have been reported. This Utility Gene Test was prepared on the basis of an analysis of the literature and existing diagnostic protocols. It is useful for confirming diagnosis, as well as for differential diagnosis, couple risk assessment and access to clinical trials.
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Details
1 MAGI’s Lab, Rovereto, Italy
2 MAGI Euregio, Bolzano, Italy
3 Center for Vascular Malformations, “Stefan Belov”, Clinical Institute Humanitas “Mater Domini”, Castellanza (Varese), Italy
4 Department of Clinical Medicine and Surgery at University of Naples Federico II, Naples, Italy
5 Department of Pharmaceutical Sciences, University of Perugia, Perugia, Italy
6 Department of Medical Genetics, Erciyes University Medical School, Kayseri, Turkey
7 MAGI’s Lab, Rovereto, Italy; MAGI Euregio, Bolzano, Italy