{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,18]],"date-time":"2026-10-18T00:53:12Z","timestamp":1792284792104,"version":"4.4.0"},"reference-count":5,"publisher":"SAGE Publications","issue":"3","license":[{"start":{"date-parts":[[1987,7,1]],"date-time":"1987-07-01T00:00:00Z","timestamp":552096000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Child Neurol"],"published-print":{"date-parts":[[1987,7]]},"abstract":"<jats:p>Encephalocraniocutaneous lipomatosis is a distinct clinical syndrome characterized by unilateral cerebral malformations and ipsilateral scalp, face, and eye lesions. The cutaneous lesions are confined to the head. The central nervous system lesions consist in part of cerebral hemiatrophy, porencephaly, and defective opercularization of the insula. The intracranial lesions and clinical symptomatology are progressive, and appear, in part, to have a vascular pathogenesis. This suggests that a primary defect in the formation of tissues derived from embryonic mesenchyme may be responsible for the syndrome and that tissues derived from ectoderm may be secondarily affected. ( J Child Neurol 1987;2:186-193).<\/jats:p>","DOI":"10.1177\/088307388700200303","type":"journal-article","created":{"date-parts":[[2008,6,3]],"date-time":"2008-06-03T05:13:24Z","timestamp":1212470004000},"page":"186-193","source":"Crossref","is-referenced-by-count":39,"title":["Encephalocraniocutaneous Lipomatosis"],"prefix":"10.1177","volume":"2","author":[{"given":"Marvin A.","family":"Fishman","sequence":"first","affiliation":[{"name":"Departments of Pediatrics and Neurology, Baylor College of Medicine, Texas Children's Hospital, Houston, TX"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[1987,7,1]]},"reference":[{"key":"atypb1","doi-asserted-by":"publisher","DOI":"10.1001\/archneur.1970.00480200050005"},{"key":"atypb2","doi-asserted-by":"crossref","first-page":"580","DOI":"10.1542\/peds.61.4.580","volume":"61","author":"Fishman MA","year":"1978","journal-title":"Pediatrics"},{"key":"atypb3","unstructured":"Alexander GL : Sturge Weber Syndrome, in Vinken PJ, Bruyn GW (eds): Handbook of Clinical Neurology, Vol 14, The Phakomatoses . New York, American Elsevier Publishing Co, 1972, pp 228-229."},{"key":"atypb4","unstructured":"deRecondo J. , Haguenau M.: Neuropathologic survey of the phakomatoses and allied disorders, in Vinken PJ, Bruyn GW (eds): Handbook of Clinical Neurology, Vol 14, The Phakomatoses . New York, American Elsevier Publishing Co, 1972, pp 19-100."},{"key":"atypb5","first-page":"1","volume":"92","author":"Bannayan GA","year":"1971","journal-title":"Arch Pathol"}],"container-title":["Journal of Child Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/088307388700200303","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1177\/088307388700200303","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,4,29]],"date-time":"2026-04-29T20:36:01Z","timestamp":1777494961000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.sagepub.com\/doi\/10.1177\/088307388700200303"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1987,7]]},"references-count":5,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1987,7]]}},"alternative-id":["10.1177\/088307388700200303"],"URL":"https:\/\/doi.org\/10.1177\/088307388700200303","relation":{},"ISSN":["0883-0738","1708-8283"],"issn-type":[{"value":"0883-0738","type":"print"},{"value":"1708-8283","type":"electronic"}],"subject":[],"published":{"date-parts":[[1987,7]]}}}