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She also had bilateral posterior embryotoxon, left corneal opacity (Peters anomaly), and cutis aplasia of the left scalp. All of these defects may have occurred as a result of disruption of the blood supply caused by NF1 vasculopathy prenatally. This constellation of vascular anomalies has not been previously reported in a patient with NF1. \u00a9 2010 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.a.33788","type":"journal-article","created":{"date-parts":[[2010,12,23]],"date-time":"2010-12-23T00:33:28Z","timestamp":1293064408000},"page":"380-385","source":"Crossref","is-referenced-by-count":11,"title":["Cerebrovasculopathy in NF1 associated with ocular and scalp defects"],"prefix":"10.1002","volume":"155","author":[{"given":"Matt","family":"Smith","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Manraj K.S.","family":"Heran","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mary B.","family":"Connolly","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Harindar 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