Second trimester fetal MRI of the brain: Through the ground glass
Fetal MRI is an important tool for the prenatal diagnosis of brain malformations and is often
requested after second‐trimester ultrasonography reveals a possible abnormality. Despite …
requested after second‐trimester ultrasonography reveals a possible abnormality. Despite …
Fetal neurology: from prenatal counseling to postnatal follow-up
B Scelsa - Diagnostics, 2022 - mdpi.com
Brain abnormalities detected in fetal life are being increasingly recognized. Child
neurologists are often involved in fetal consultations, and specific fetal neurology training …
neurologists are often involved in fetal consultations, and specific fetal neurology training …
Congenital brain malformations-update on newer classification and genetic basis
A Sarma, S Pruthi - Seminars in Roentgenology, 2023 - Elsevier
Congenital malformations of the brain are caused by disruption of normal development
during embryonic or fetal life and are present from birth. Increasing investigation of the …
during embryonic or fetal life and are present from birth. Increasing investigation of the …
Dandy-Walker Phenotype with Brainstem Involvement: 2 Distinct Subgroups with Different Prognosis
BACKGROUND AND PURPOSE: Although cardinal imaging features for the diagnostic
criteria of the Dandy-Walker phenotype have been recently defined, there is a large range of …
criteria of the Dandy-Walker phenotype have been recently defined, there is a large range of …
The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders
Inherited glycosylphosphatidylinositol deficiency disorders (IGDs) are a group of rare
multisystem disorders arising from pathogenic variants in glycosylphosphatidylinositol …
multisystem disorders arising from pathogenic variants in glycosylphosphatidylinositol …
Prenatal assessment of brain malformations on neuroimaging: an expert panel review
I Pogledic, K Mankad, M Severino, T Lerman-Sagie… - Brain, 2024 - academic.oup.com
Brain malformations represent a heterogeneous group of abnormalities of neural
morphogenesis, often associated with aberrations of neuronal connectivity and brain …
morphogenesis, often associated with aberrations of neuronal connectivity and brain …
Fetal and neonatal outcomes of posterior fossa anomalies: a retrospective cohort study
H Alsehli, SM Alshahrani, S Alzahrani, F Ababneh… - Scientific Reports, 2024 - nature.com
The primary aim of this study was to estimate the incidence of posterior fossa anomalies
(PFA) and assess the associated outcomes in King Abdulaziz Medical City (KAMC), Riyadh …
(PFA) and assess the associated outcomes in King Abdulaziz Medical City (KAMC), Riyadh …
Undifferentiated psychosis or schizophrenia associated with vermis‐predominant cerebellar hypoplasia
AC Leslie, MP Ward, WB Dobyns - American Journal of Medical …, 2024 - Wiley Online Library
Schizophrenia (SCZ) is a well‐studied neuropsychiatric condition that has been shown to
have a high degree of genetic heritability. Still, little data on the specific genetic risk variants …
have a high degree of genetic heritability. Still, little data on the specific genetic risk variants …
Not Dandy–Walker variant: a review of prominent retrocerebellar cerebrospinal space in children
The prominent retrocerebellar cerebrospinal fluid (CSF) space can be frequently
encountered on paediatric neuroimaging studies. In cases involving abnormal vermian …
encountered on paediatric neuroimaging studies. In cases involving abnormal vermian …
Neuroimaging Findings in Axenfeld-Rieger Syndrome: A Case Series
S White, A Taranath, P Hanagandi… - American Journal …, 2023 - Am Soc Neuroradiology
Axenfeld-Rieger syndrome is an autosomal dominant condition associated with
multisystemic features including developmental anomalies of the anterior segment of the …
multisystemic features including developmental anomalies of the anterior segment of the …