Main Article Content
Mutations in the RASA-1 gene underlie several related disorders of vasculogenesis. Capillary malformation-arteriovenous malformation (CM-AVM) is one such entity and was recently encountered in a neonate who demonstrated its clinical and radiologic features. A single mutation in the RASA-1 gene was detected.
A novel flow reduction strategy was employed to a large AVM affecting the patient’s upper limb. The imaging findings, surgical procedure and patient’s improved post-operative state are described.
How to Cite
BEHR, Gerald G et al. CM-AVM syndrome in a neonate: case report and treatment with a novel flow reduction strategy. Vascular Cell, [S.l.], v. 4, n. 1, p. 19, nov. 2012. ISSN 2045-824X. Available at: <https://vascularcell.com/index.php/vc/article/view/10.1186-2045-824X-4-19>. Date accessed: 20 jan. 2022. doi: http://dx.doi.org/10.1186/2045-824X-4-19.