Results 61 to 70 of about 1,803 (152)

Clinical manifestations and neuroimaging findings of schizencephaly in children [PDF]

open access: yes, 2009
PURPOSE: Schizencephaly is a uncommon congenital brain anomaly characterized by congenital clefts spanning the cerebral hemispheres from pial surface to lateral ventricles and lined by gray matter.
이영목, 이준수, 김흥동
core   +1 more source

Hydranencephaly in Neonate With Prenatal Exposure to Alcohol During Pregnancy

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Hydranencephaly (HE) is a rare congenital condition characterized by near‐total absence of the cerebral hemispheres, replaced by cerebrospinal fluid, most commonly resulting from in utero bilateral internal carotid artery occlusion; although maternal alcohol consumption is associated with fetal neurodevelopmental abnormalities, its direct role
Dibya Raj Chaudhary   +3 more
wiley   +1 more source

Literature Review: Sonographic Diagnosis of Schizencephaly

open access: yes, 2010
Schizencephaly is a congenital brain malformation in which clefts develop in the cerebral hemispheres. This aberration may be described as open lip (type I) or closed lip (type II) and may be further expressed as unilateral or bilateral.
Steven M. Penny   +2 more
core   +1 more source

Interictal and seizure‐onset scalp electroencephalographic patterns in malformations of cortical development

open access: yesEpilepsia, Volume 67, Issue 6, Page 2979-2991, June 2026.
Abstract Objective Malformations of cortical development (MCDs) are a frequent cause of drug‐resistant epilepsy and a common indication for resective epilepsy surgery. As magnetic resonance imaging (MRI) lacks sensitivity for subtle MCDs, supplemental diagnostic tools are needed.
Lubna Shakhatreh   +10 more
wiley   +1 more source

Neuroimaging of septo-optic dysplasia-plus with midbrain hypoplasia and ophthalmoplegia

open access: yeseNeurologicalSci, 2020
Septo-optic dysplasia is a rare brain malformation that can be associated with anomalous cortical development, such as schizencephaly, which is referred to as septo-optic dysplasia plus.
Colin Y. Wang, Daniel T. Ginat
doaj   +1 more source

Early Maturation of Heart Rate Variability in Very Preterm Infants Depends on Neonatal Factors and Is Associated With Neurodevelopmental Risk

open access: yesActa Paediatrica, Volume 115, Issue 6, Page 1191-1201, June 2026.
ABSTRACT Aim This study investigated central autonomic network maturation deviations using a previously defined machine learning model set to estimate a functional maturation age (FMA) from heart rate variability (HRV) analysis. We investigated whether these deviations were associated with maternal, fetal, perinatal, or postnatal complications and with
Léa Bonneau   +9 more
wiley   +1 more source

Frontoethmoidal encephalocele presenting in concert with schizencephaly [PDF]

open access: yes, 2018
Background: Schizencephaly is a rare defect which is identified as clefts that are lined with grey matter extending from the ependyma of the cerebral ventricles to the pia mater.
Bukhari, Syed Sarmad   +2 more
core  

A case of schizencephaly associated with skeletal deformities and abnormal eye movements

open access: yes, 2005
Schizencephaly is an extremely rare developmental disorder characterized by abnormal clefts in the brain's cerebral hemispheres. The major clinical features are mental-motor retardation, seizures, microcephaly, and hemiparesis or quadriparesis.
Koc Z.   +3 more
core   +1 more source

The Management of Congenital Cytomegalovirus Infection in an Era of Universal Newborn CMV Screening

open access: yesReviews in Medical Virology, Volume 36, Issue 3, May 2026.
ABSTRACT The most common infectious disease responsible for paediatric developmental disability is congenital infection with human cytomegalovirus (cCMV). Many serious sequelae are caused by cCMV, including microcephaly, intracranial calcifications, neuronal migration defects, seizure disorders, developmental delay, and sensorineural hearing loss (SNHL)
Emily R. Harrison   +2 more
wiley   +1 more source

Home - About - Disclaimer - Privacy