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Washington University Experience | MYELIN (NON-IMMUNE MEDIATED) | Retinal Vasculopathy with Cerebral Leukoencephalopathy (RVCL, TREX1 Mutation) | 18D1 TREX1 Disease (Case 18) H&E N23 WM

18D1 TREX1 Disease (Case 18) H&E N23 WM
This is an additional whole mount section of one of the focally calcified frontal lobe lesions and shows substantial cortical pathology as well as pallor of the white matter, sparing the U fibers. (H&E)



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