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This syndrome is a multiple congenital anomalies\/mental retardation and overgrowth disorder comprising macrocephaly, cutis marmorata, vascular marks of lip and\/or philtrum, syndactyly, hemihypertrophy, CNS anomalies, and developmental delay. Based on the findings in our 6 patients and on 69 patients previously reported we listed the very frequent (observed in &gt;75%), frequent (25\u201375%), and less frequent (&gt;25%) components of the syndrome. \u00a9 2004 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.a.30235","type":"journal-article","created":{"date-parts":[[2004,8,3]],"date-time":"2004-08-03T13:00:23Z","timestamp":1091538023000},"page":"45-51","source":"Crossref","is-referenced-by-count":84,"title":["Macrocephaly\u2010cutis marmorata telangiectatica congenita: Report of six new patients and a review"],"prefix":"10.1002","volume":"130A","author":[{"given":"Pablo","family":"Lapunzina","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alba","family":"Gair\u00ed","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alicia","family":"Delicado","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M. 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