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The external genitalia were asymmetric and ambiguous with normal uterus and ovaries visualized by ultrasound. The anomalies are compatible with previously reported cases of Al\u2010Awadi\/Raas\u2010Rothschild\/Schinzel (AARRS) phocomelia, an autosomal recessive disorder with <jats:italic>WNT7<\/jats:italic> gene mutations documented in one family. We suggest that AARRS phocomelia, Fuhrmann syndrome, and similar conditions comprise a spectrum, and that the anomaly pattern derives from serial action of the same signal pathways within primary (e.g., the major axes), secondary (e.g., heart or limb primordia), and\/or local (e.g., tibial\u2013fibular differentiation) developmental fields. \u00a9 2009 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.a.32890","type":"journal-article","created":{"date-parts":[[2009,6,15]],"date-time":"2009-06-15T19:01:37Z","timestamp":1245092497000},"page":"1494-1498","source":"Crossref","is-referenced-by-count":5,"title":["Al\u2010Awadi\/Raas\u2010Rothschild\/Schinzel (AARRS) phocomelia syndrome: Case report and developmental field 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