@article {Beavers:2018:2637-8329:22,
title = "Infantile Vanishing White Matter Disease: A Case Report",
journal = "Neurographics",
parent_itemid = "infobike://asnr/ng",
publishercode ="asnr",
year = "2018",
volume = "8",
number = "1",
publication date ="2018-02-01T00:00:00",
pages = "22-24",
itemtype = "ARTICLE",
issn = "2637-8329",
eissn = "2637-8329",
url = "https://asnr.publisher.ingentaconnect.com/content/asnr/ng/2018/00000008/00000001/art00004",
doi = "doi:10.3174/ng.9170223",
keyword = "VWM = vanishing white matter",
author = "Beavers, K.M. and Flores, M.A. and Dagli, A.I. and Messina, S.A.",
abstract = "Vanishing white matter disease is a progressive inherited leukodystrophy with a poor prognosis in its infantile form. We present a case that demonstrates the inverse correlation between disease severity and age of onset in a patient with an aggressive variant, resulting in rapid clinical
decline. This report aims to highlight critical imaging findings that are necessary to establish a timely diagnosis and properly guide clinicians in vanishing white matter disease. Key imaging findings, differential diagnoses, and genetic abnormalities are reviewed.",
}