{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,11,14]],"date-time":"2022-11-14T05:28:51Z","timestamp":1668403731154},"reference-count":15,"publisher":"Journal of Neurosurgery Publishing Group (JNSPG)","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[1971,6]]},"abstract":"<jats:p content-type=\"fine-print\">\u2713 A family with craniofacial dysostosis affecting a father and his monozygotic twin sons is described. The father had no surgery until linear craniectomy when 3 years old; he is of normal intelligence but legally blind. Prophylactic coronal craniectomy and orbital decompression were done on the twins. One had an uncomplicated course and is developing normally. The other developed neonatal meningitis and ventriculitis with secondary hydrocephalus, plus poor vision and retarded development.<\/jats:p>","DOI":"10.3171\/jns.1971.34.6.0779","type":"journal-article","created":{"date-parts":[[2009,5,7]],"date-time":"2009-05-07T14:36:04Z","timestamp":1241706964000},"page":"779-782","source":"Crossref","is-referenced-by-count":1,"title":["Surgical treatment of craniofacial dysostosis in monozygotic twins"],"prefix":"10.3171","volume":"34","author":[{"given":"Jane C. S.","family":"Perrin","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Martin H.","family":"Weiss","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"David","family":"Yashon","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"1754","reference":[{"key":"b1","series-title":"J Neurosurg","doi-asserted-by":"publisher","first-page":"229","DOI":"10.3171\/jns.1965.22.3.0229","article-title":"Craniosynostosis: a survey of 204 cases.","volume":"22","author":"Anderson","year":"1965"},{"key":"b2","series-title":"Acta Paediat Scand","doi-asserted-by":"publisher","first-page":"47","DOI":"10.1111\/j.1651-2227.1968.tb07285.x","article-title":"Craniosynostosis: review of the literature and indications for surgery.","volume":"57","author":"Andersson","year":"1968"},{"key":"b3","series-title":"Med Press Circ","first-page":"118","article-title":"Hereditary cranio-facial dysostosis, or Crouzon's disease.","volume":"195","author":"Atkinson","year":"1937"},{"key":"b4","series-title":"The Pathology of the Human Placenta.","first-page":"159","author":"Benirschke","year":"1967"},{"key":"b5","series-title":"Bull Soc Med Hop Paris","first-page":"545","article-title":"Dysostose cranio-faciale h\u00e9r\u00e9ditaire.","volume":"33","author":"Crouzon","year":"1912"},{"key":"b6","series-title":"Pediatrics","doi-asserted-by":"publisher","first-page":"98","DOI":"10.1542\/peds.23.1.98","article-title":"Craniofacial dysostosis: Crouzon's disease.","volume":"23","author":"Dodge","year":"1959"},{"key":"b7","series-title":"Pediatrics","doi-asserted-by":"publisher","first-page":"90","DOI":"10.1542\/peds.5.1.90","article-title":"Cranio-facial dysostosis of Crouzon: report of a case in which the malformation occurred in four generations.","volume":"5","author":"Flippen","year":"1950"},{"key":"b8","series-title":"Nord Med","first-page":"993","article-title":"Cranio-facial dysostosis as dominant hereditary disease.","volume":"18","author":"Fogh-Anderson","year":"1943"},{"key":"b9","series-title":"Endokrinologie","first-page":"255","article-title":"Dysostosis craniofacialis hereditaria.","volume":"13","author":"G\u00fcnther","year":"1933"},{"key":"b10","series-title":"Surgery (St Louis)","first-page":"518","article-title":"Clinical studies in craniosynostosis: analysis of fifty cases and description of a method of surgical treatment.","volume":"24","author":"Ingraham","year":"1948"},{"key":"b11","series-title":"Neurosurgery of Infancy and Childhood.","first-page":"156","author":"Matson","year":"1969"},{"key":"b12","series-title":"Amer J Ophthal","doi-asserted-by":"publisher","first-page":"500","DOI":"10.1016\/0002-9394(52)91316-0","article-title":"Hereditary craniofacial dysplasia.","volume":"35","author":"Pinkerton","year":"1952"},{"key":"b13","series-title":"Pediatrics","doi-asserted-by":"publisher","first-page":"107","DOI":"10.1542\/peds.23.1.107","article-title":"Craniofacial dysostosis of Crouzon: a case report and pedigree with emphasis on heredity.","volume":"23","author":"Schiller","year":"1959"},{"key":"b14","series-title":"Pediatrics","doi-asserted-by":"publisher","first-page":"829","DOI":"10.1542\/peds.41.4.829","article-title":"Craniosynostosis: a review of 519 surgical patients.","volume":"41","author":"Shillito","year":"1968"},{"key":"b15","series-title":"Arch Dis Child","doi-asserted-by":"publisher","first-page":"375","DOI":"10.1136\/adc.41.218.375","article-title":"Cranio-facial dysostosis in a Dorset family.","volume":"41","author":"Vulliamy","year":"1966"}],"container-title":["Journal of Neurosurgery"],"original-title":[],"link":[{"URL":"https:\/\/thejns.org\/view\/journals\/j-neurosurg\/34\/6\/article-p779.xml","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/thejns.org\/downloadpdf\/journals\/j-neurosurg\/34\/6\/article-p779.xml","content-type":"text\/html","content-version":"vor","intended-application":"syndication"},{"URL":"https:\/\/thejns.org\/downloadpdf\/journals\/j-neurosurg\/34\/6\/article-p779.xml","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2022,11,13]],"date-time":"2022-11-13T05:31:21Z","timestamp":1668317481000},"score":1,"resource":{"primary":{"URL":"https:\/\/thejns.org\/view\/journals\/j-neurosurg\/34\/6\/article-p779.xml"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1971,6]]},"references-count":15,"journal-issue":{"issue":"6"},"URL":"https:\/\/doi.org\/10.3171\/jns.1971.34.6.0779","relation":{},"ISSN":["0022-3085"],"issn-type":[{"value":"0022-3085","type":"print"}],"subject":[],"published":{"date-parts":[[1971,6]]}}}