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We describe a 30-year-old man with depigmented, bilateral hypertrichosis and dilated follicular orifices following Blaschko\u2019s lines associated with cerebral and ocular malformations. The findings suggest a previously unreported neurocutaneous, autosomal lethal gene syndrome from the group of epidermal naevus syndromes.<\/jats:p>","DOI":"10.1046\/j.1365-2133.2000.03551.x","type":"journal-article","created":{"date-parts":[[2003,3,11]],"date-time":"2003-03-11T05:27:52Z","timestamp":1047360472000},"page":"1204-1207","source":"Crossref","is-referenced-by-count":29,"title":["Depigmented hypertrichosis following Blaschko\u2019s lines associated with cerebral and ocular malformations: a new neurocutaneous, autosomal lethal gene syndrome from the group of epidermal naevus syndromes?"],"prefix":"10.1093","volume":"142","author":[{"given":"S.","family":"Schauder","sequence":"first","affiliation":[{"name":"Department of Dermatology, Georg-August-University Goettingen, von-Siebold-Stra\u00dfe 3, D-37075 Goettingen, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"F.","family":"Hanefeld","sequence":"additional","affiliation":[{"name":"Department of Neuropaediatrics, Georg-August-University, Goettingen, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"U.M.","family":"Noske","sequence":"additional","affiliation":[{"name":"Department of Ophthalmology, Georg-August-University, Goettingen, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"B.","family":"Zoll","sequence":"additional","affiliation":[{"name":"Department of Human Genetics, Georg-August-University, Goettingen, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","published-online":{"date-parts":[[2000,6,1]]},"reference":[{"key":"2023013010223699000_b1","doi-asserted-by":"crossref","first-page":"542","DOI":"10.1046\/j.1365-2133.1999.02729.x","article-title":"Aplasia cutis congenita, uvula bifida and bilateral retinal dystrophy in a girl with naevus sebaceous syndrome","volume":"140","author":"H\u00f6gler","year":"1999","journal-title":"Br J Dermatol"},{"key":"2023013010223699000_b2","doi-asserted-by":"crossref","first-page":"324","DOI":"10.1002\/(SICI)1096-8628(19990806)85:4<324::AID-AJMG2>3.0.CO;2-O","article-title":"Functional X-chromosomal mosaicism of the skin: Rudolf Happle and the lines of Alfred Blaschko","volume":"85","author":"Traupe","year":"1999","journal-title":"Am J Med Genet"},{"key":"2023013010223699000_b3","doi-asserted-by":"crossref","first-page":"155","DOI":"10.2340\/0001555572155156","article-title":"Linear alopecia mucinosa along Blaschko lines","volume":"72","author":"Tosti","year":"1992","journal-title":"Acta Derm Venereol"},{"key":"2023013010223699000_b4","doi-asserted-by":"crossref","first-page":"342","DOI":"10.1002\/(SICI)1096-8628(19990806)85:4<342::AID-AJMG6>3.0.CO;2-8","article-title":"Cutaneous mosaicism of lethal mutations","volume":"85","author":"Hamm","year":"1999","journal-title":"Am J Med Genet"},{"key":"2023013010223699000_b5","doi-asserted-by":"crossref","first-page":"346","DOI":"10.1002\/(SICI)1096-8628(19990806)85:4<346::AID-AJMG7>3.0.CO;2-1","article-title":"Hypomelanosis of Ito: No entity, but a cutaneous sign of mosaicism","volume":"85","author":"Kuester","year":"1999","journal-title":"Am J Med Genet"},{"key":"2023013010223699000_b6","doi-asserted-by":"crossref","first-page":"330","DOI":"10.1002\/(SICI)1096-8628(19990806)85:4<330::AID-AJMG3>3.0.CO;2-M","article-title":"Cytogenic and molecular evidence for cutaneous mosaicism: the ectodermal origin of Blaschko lines","volume":"85","author":"Moss","year":"1999","journal-title":"Am J Med Genet"},{"key":"2023013010223699000_b7","doi-asserted-by":"crossref","first-page":"550","DOI":"10.1016\/0190-9622(91)70238-W","article-title":"How many epidermal nevus syndromes exist? 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