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Washington University Experience | DEVELOPMENTAL MALFORMATIONS | Heterotopia - Leptomeningeal | 5A1 Heterotopia, leptomeningeal (Galloway-Mowat Syndrome, AANP 1994, Case 9) H&E X0.5
Images from a previous diagnostic slide session of the AANP (1994, case 9) from a patient with Galloway-Mowat syndrome, an autosomal recessive neurodegenerative disease characterized by microcephaly. In the case shown there is mostly a migrational disorder with numerous leptomeningeal heterotopias (arrows) that form prominent connections with underlying cortex in this section of frontal lobe (H&E)
