PT - JOURNAL ARTICLE AU - W J Carroll AU - W W Woodruff AU - T E Cadman TI - MR findings in oculocerebrorenal syndrome. DP - 1993 Mar 01 TA - American Journal of Neuroradiology PG - 449--451 VI - 14 IP - 2 4099 - http://www.ajnr.org/content/14/2/449.short 4100 - http://www.ajnr.org/content/14/2/449.full SO - Am. J. Neuroradiol.1993 Mar 01; 14 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.