Results 41 to 50 of about 1,803 (152)

Giant bilateral open-lip schizencephaly [Esquizencefalia bilateral gigante de labio abierto]

open access: yes, 2022
Schizencephaly is a rare congenital brain malformation characterized by clefts in the cerebral cortex, it is classified in Type I (open lip) and Type II (close-lip). Patients with schizencephaly present seizures, hydrocephalus, motor and mental deficits.
Sarango-Amay K.   +3 more
core   +1 more source

Unilateral open-lip schizencephaly with tonsillar herniation in a preterm infant

open access: yesJournal of Pediatric Neurosciences, 2019
Schizencephaly is a rare type of neuronal migration disorder characterized by the presence of a cerebral hemispheric cleft that extends from lateral ventricles to the cortical surface of the brain. We report a rare case of prenatally diagnosed unilateral
Juan Carlos Gonzalez   +4 more
doaj   +1 more source

Schizencephaly: a rare case with early diagnosis, management and review of literature [PDF]

open access: yes, 2023
Schizencephaly or split brain is an uncommon congenital disorder of cerebral cortical development, belonging to the group of cell migration defects. It is characterized by the presence of a cleft in the brain extending from the surface of the piamater to
Agarwal, Megha   +4 more
core   +1 more source

Schizencephaly and psychosis

open access: yes, 2011
Schizencephaly is an uncommon congenital disorder of cerebral cortical development, defined as a gray matter-lined cleft extending from the pial surface to the ventricle.
R.S. Dhillon   +7 more
core   +1 more source

Schizencephaly: A case report and review of literature

open access: yesNigerian Postgraduate Medical Journal, 2016
Schizencephaly is a congenital condition characterized by cerebrospinal fluid-filled clefts that extend from the pia surface of the cerebral hemisphere to the ependymal surface of the ventricle.
Enighe W Ugboma, C E Agi
doaj   +1 more source

Clinical significance of subclinical seizures in epilepsy presurgical evaluation: A systematic review and meta‐analysis

open access: yesEpilepsia, EarlyView.
Abstract Objective Subclinical seizures (SCSs) remain an understudied aspect of presurgical evaluation in patients with drug‐resistant epilepsy (DRE), with uncertain prevalence, distribution among epilepsy types, and predictive value for surgical outcomes.
Pilar Bosque‐Varela   +6 more
wiley   +1 more source

Febrile status epilepticus and epileptogenesis: The FEBSTAT study

open access: yesEpilepsia Open, EarlyView.
Abstract The multicenter FEBSTAT study (Consequences of Prolonged Febrile Seizures in Childhood: https://grantome.com/grant/NIH/R37‐NS043209‐12; PI S. Shinnar) examined the outcome of febrile status epilepticus (FSE) in over 200 prospectively enrolled infants, with many followed for 10 years after FSE.
Darrell V. Lewis   +14 more
wiley   +1 more source

Trio-Based Whole-Exome Sequencing Identifies a De novo EFNB1 Mutation as a Genetic Cause in Female Infant With Brain Anomaly and Developmental Delay

open access: yesFrontiers in Pediatrics, 2020
Background: Craniofrontonasal syndrome is a rare, X-linked disorder in which heterozygous females ironically reported the majority of patients and is caused by in the EFNB1 gene located at chromosome Xq13.1.
Ji Yoon Han   +5 more
doaj   +1 more source

Fetal Intracranial Hemorrhage: What to Tell Expecting Parents?

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Fetal intracranial hemorrhage (ICH) is a rare but serious prenatal diagnosis, and counseling affected families remains challenging. In this narrative review, we summarize current evidence on the classification, epidemiology, etiology, diagnosis and neurodevelopmental outcomes of fetal ICH, with a primary focus on intraventricular hemorrhage ...
Shiri Shinar, Yada Kunpalin, Elka Miller
wiley   +1 more source

Esquisencefalia. Estudio de 16 pacientes

open access: yesNeurología, 2012
Resumen: Objetivo: Presentar 16 pacientes con esquisencefalia y afectación neurológica recalcando sus características clínicas y de imagen. Material y métodos: Son 16 pacientes, 8 varones y 8 mujeres, todos ellos con edades por debajo de los 3 años al ...
I. Pascual-Castroviejo   +4 more
doaj   +1 more source

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