Article
Arterial Tortuosity Syndrome: homozygosity for two novel and one recurrent SLC2A10 missense mutations in three families with severe cardiopulmonary complications in infancy and a literature review.
BMC medical genetics - 6 Nov 2014
Ritelli Marco, Chiarelli Nicola, Dordoni Chiara, Reffo Elena, Venturini Marina, Quinzani Stefano, Monica Matteo Della, Scarano Gioacchino, Santoro Giuseppe, Russo Maria Giovanna, Calzavara-Pinton Piergiacomo, Milanesi Ornella, Colombi Marina
Abstract excerpt
BACKGROUND: Arterial Tortuosity Syndrome (ATS) is a very rare autosomal recessive connective tissue disorder (CTD) characterized by tortuosity and elongation of the large- and medium-sized arteries and a propensity for aneurysm formation and vascular dissection. During infancy, children frequently present the involvement of the pulmonary arteries (elongation, tortuosity, stenosis) with dyspnea and cyanosis. Other...
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