RT Journal Article SR Electronic T1 MR findings in oculocerebrorenal syndrome. JF American Journal of Neuroradiology JO Am. J. Neuroradiol. FD American Society of Neuroradiology SP 449 OP 451 VO 14 IS 2 A1 Carroll, W J A1 Woodruff, W W A1 Cadman, T E YR 1993 UL http://www.ajnr.org/content/14/2/449.abstract AB Oculocerebrorenal syndrome is an X-linked recessive disorder characterized by congenital ocular abnormalities, mental retardation, renal disease, and metabolic bone disease. We report a case of oculocerebrorenal syndrome and, using T1-, proton density-, and T2-weighted imaging sequences, are able to characterize two distinct white matter abnormalities: one lesion is punctate and has signal characteristics that parallel that of cerebrospinal fluid; a second lesion, found in association with the first, consists of patchy white matter abnormalities that are hypointense on T1-weighted images but hyperintense on proton density- and T2-weighted images.