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Fig. 4 | Orphanet Journal of Rare Diseases

Fig. 4

From: Galloway-Mowat syndrome in Taiwan: OSGEP mutation and unique clinical phenotype

Fig. 4

Images of fetal ultrafast MRI. a Patient III-1 at 34 weeks of gestation shows pachygyria, especially in the bilateral frontal lobes, and poor myelination of the white matter (b) Patient III-2 at 32 weeks of gestation shows hypomelination with T2 hyperintensity in bilateral cerebral white matter, particularly both temporal lobes (arrows), and prominence of retrocerebellar cisterns due to cerebellar atrophy (arrowheads)

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