Fig.1From: Novel MTR compound-heterozygous mutations in a Chinese girl with HHcy due to methionine synthase deficiency, cblG: a case reportA 24-h video-electroencephalographic showed multifocal sharp waves, mainly during sleep and two spasms during wakefulness. B Magnetic resonance imaging showed widened peripheral cerebrospinal fluid spaces, slightly deepened cerebral sulcus, decreased brain parenchyma, and corpus callosum hypoplasiaBack to article page