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Based on the evolution of clinical features in this infant, we suggest that our case, as well as that reported by Van Allen and Myhre, is an example of unusually severe Goltz syndrome. \u00a9 2002 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.10456","type":"journal-article","created":{"date-parts":[[2002,10,6]],"date-time":"2002-10-06T11:34:39Z","timestamp":1033904079000},"page":"370-379","source":"Crossref","is-referenced-by-count":16,"title":["Probable identity of Goltz syndrome and Van Allen\u2010Myhre syndrome: Evidence from phenotypic evolution"],"prefix":"10.1002","volume":"110","author":[{"given":"Susan","family":"Hancock","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Peter","family":"Pryde","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christine","family":"Fong","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jane E.","family":"Brazy","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Katharina","family":"Stewart","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Amy","family":"Favour","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Richard M.","family":"Pauli","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2002,5,16]]},"reference":[{"key":"e_1_2_5_2_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320300407"},{"key":"e_1_2_5_3_1","first-page":"702","article-title":"Agenesis of the corpus callosum in a case of focal dermal hypoplasia","volume":"37","author":"Baughman FA","year":"1970","journal-title":"Mt Sinai J Med"},{"key":"e_1_2_5_4_1","doi-asserted-by":"publisher","DOI":"10.1002\/pd.1970070803"},{"key":"e_1_2_5_5_1","doi-asserted-by":"crossref","first-page":"314","DOI":"10.3928\/0191-3913-19821101-08","article-title":"Focal dermal hypoplasia: ocular manifestations in a male","volume":"19","author":"Broughton WL","year":"1982","journal-title":"J Pediatr Ophthalmol Strabismus"},{"key":"e_1_2_5_6_1","first-page":"1354","article-title":"Focal dermal hypoplasia","volume":"4","author":"Daly JF","year":"1968","journal-title":"Cutis"},{"key":"e_1_2_5_7_1","first-page":"37","article-title":"Focal dermal hypoplasia (Goltz syndrome) in a male","volume":"31","author":"Fryns JP","year":"1978","journal-title":"Acta Paediatr Belg"},{"key":"e_1_2_5_8_1","doi-asserted-by":"publisher","DOI":"10.1302\/0301-620X.52B4.629"},{"key":"e_1_2_5_9_1","doi-asserted-by":"publisher","DOI":"10.2214\/ajr.110.3.561"},{"key":"e_1_2_5_10_1","doi-asserted-by":"crossref","first-page":"1108","DOI":"10.1001\/archderm.1992.01680180102015","article-title":"Focal dermal hypoplasia syndrome. 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