Mikrohydranenzephalie
Prenatal
diagnosis of fetal microhydranencephaly: a case report and literature review. Prenatal fetal 3-dimensional computed tomography (3D-CT) and magnetic resonance imaging (MRI) scans. a and b 3D-CT images at 34 weeks of gestation showing the presence of a fetal skull, a prominent occipital bone, and a sloping forehead. c T2-weighted sagittal image of an MRI scan showing a cerebral sickle, cerebellar tent, a defect of the cerebrum, a hypoplastic cerebellum, a normal brain stem, and excess cerebrospinal fluid
Prenatal
diagnosis of fetal microhydranencephaly: a case report and literature review. Magnetic resonance imaging (MRI) findings of the infant’s head. a T2-weighted sagittal image. b T2-weighted coronal image. On day 32 after birth, an MRI scan showed the absence of a cerebrum and a membranous structure in the region of the cerebrum with hydrocephalus
Assoziationen und Differentialdiagnosen zu Mikrohydranenzephalie: