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Fig. 3 | BMC Medical Genomics

Fig. 3

From: Novel pathogenic OCRL mutations and genotype–phenotype analysis of Chinese children affected by oculocerebrorenal syndrome: two cases and a literature review

Fig. 3

Brain MRI and renal pathological changes of patient 2 at the age of 7 months. a Note the presence of ventriculomegaly, white matter shrinkage, leukoaraiosis, cerebellar hypoplasia, and a large cistern magna cyst. b Note the presence of interstitial focal fibrosis with infiltration of focal mononuclear cells and mild mesangial proliferation

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BMC Medical Genomics

ISSN: 1755-8794

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