@article {Macnojia:2025:2637-8329:218,
title = "Encephalocraniocutaneous Lipomatosis: A Case Series of Radiologic Findings and Literature Review",
journal = "Neurographics",
parent_itemid = "infobike://asnr/ng",
publishercode ="asnr",
year = "2025",
volume = "15",
number = "3",
publication date ="2025-07-01T00:00:00",
pages = "218-228",
itemtype = "ARTICLE",
issn = "2637-8329",
eissn = "2637-8329",
url = "https://asnr.publisher.ingentaconnect.com/content/asnr/ng/2025/00000015/00000003/art00007",
doi = "doi:10.3174/ng.2400043",
author = "Macnojia, A. and Desai, N. and Huisman, T.A.G.M. and Kralik, S. and Lequin, M. and Moeller, K. and Narayanan, S. and Patel, R. and Rauch, R. and Tran, H.B.",
abstract = "Encephalocraniocutaneous lipomatosis (ECCL) is an extremely rare congenital disorder that classically manifests with a triad of ipsilateral CNS, dermatologic, and ophthalmic involvement. Patients with the disease present with highly variable signs and symptoms with associated physical,
neurologic, and developmental complications. The goal of this article was to expand the current, predominantly case reportbased literature on ECCL by discussing the spectrum of imaging findings in a series of 8 children with a confirmed diagnosis of ECCL.",
}