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Two of the three had pyloric stenosis, two were intellectually normal, and one had academic problems but had a history of birth hypoxia. Pedigree is consistent with an autosomal recessive mode of inheritance. Lack of previous reports suggests this represents a novel syndromic form of arthrogryposis. \u00a9 2010 Wiley\u2010Liss, Inc.<\/jats:p>","DOI":"10.1002\/ajmg.a.33794","type":"journal-article","created":{"date-parts":[[2010,12,23]],"date-time":"2010-12-23T00:34:10Z","timestamp":1293064450000},"page":"297-300","source":"Crossref","is-referenced-by-count":5,"title":["Arthrogryposis, perthes disease, and upward gaze palsy: A novel autosomal recessive syndromic form of arthrogryposis"],"prefix":"10.1002","volume":"155","author":[{"given":"Fowzan S.","family":"Alkuraya","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2010,12,22]]},"reference":[{"key":"e_1_2_4_2_1","doi-asserted-by":"publisher","DOI":"10.1002\/(SICI)1096-8628(19970905)71:4<401::AID-AJMG6>3.0.CO;2-W"},{"key":"e_1_2_4_3_1","doi-asserted-by":"publisher","DOI":"10.2106\/JBJS.I.00281"},{"key":"e_1_2_4_4_1","doi-asserted-by":"publisher","DOI":"10.1136\/jnnp.49.6.686"},{"key":"e_1_2_4_5_1","doi-asserted-by":"publisher","DOI":"10.1093\/brain\/105.1.125"},{"key":"e_1_2_4_6_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.31626"},{"key":"e_1_2_4_7_1","volume-title":"Gorlin's syndromes of the head and neck","author":"Hennekam P","year":"2010"},{"key":"e_1_2_4_8_1","doi-asserted-by":"crossref","first-page":"32","DOI":"10.1007\/BF00180176","article-title":"Legg\u2013Calve\u2013Perthes' disease in the Russell\u2013Silver syndrome. 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