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He has in addition camptodactyly of all fingers and to some extent of his toes, and unusual skin pigmentations. He resembles an earlier described family from Norway in which a mother and two children showed a similar combination of signs. We present the follow\u2010up of the Norwegian family. The entity resembles the Penttinen syndrome but can be differentiated due to the early aging in the latter, which is lacking in the presently reported entity. We suggest naming this entity ocular pterygium\u2013digital keloid dysplasia. The condition follows likely an autosomal dominant pattern of inheritance. \u00a9 2014 Wiley Periodicals, Inc.<\/jats:p><\/jats:sec>","DOI":"10.1002\/ajmg.a.36713","type":"journal-article","created":{"date-parts":[[2014,8,14]],"date-time":"2014-08-14T17:17:20Z","timestamp":1408036640000},"page":"2901-2907","source":"Crossref","is-referenced-by-count":9,"title":["Ocular pterygium\u2014Digital keloid dysplasia"],"prefix":"10.1002","volume":"164","author":[{"given":"Hugo","family":"Abarca","sequence":"first","affiliation":[{"name":"Instituto Nacional de Salud del Nino Lima Peru"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anne E Christensen","family":"Mellgren","sequence":"additional","affiliation":[{"name":"Department of Ophthalmology Haukeland University Hospital Bergen Norway"},{"name":"Department of Clinical Medicine University of Bergen Bergen 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