hydrocephalus/seizures

A total of 92 patients with hydrocephalus were studied. The incidence of seizures was significantly greater in the "shunted" group (18.2% in the "non-shunted" and 65.4% in the "shunted" group). All of the shunted patients who had seizures developed them after the placement of the shunt. Left sided

> At week 32 of a pregnancy complicated by maternal seizures, fetal ultrasonography showed hydrocephalus and an intracranial hyperechoic mass identified by magnetic resonance imaging as subacute right thalamic hemorrhage, with aqueductal obstruction. Fetal intracranial bleeding may be a cause factor

202 cases of children with shunted hydrocephalus of congenital or acquired origin were studied and the incidence of seizure disorder was found to be 39%. However in only 17% of cases was the seizure disorder found to be persistent. Focal seizures were rarer than expected. If focal seizures were

Mutations in the LGI1 gene predispose to a hereditary epilepsy syndrome and is the first gene associated with this disease which does not encode an ion channel protein. In zebrafish, there are two paralogs of the LGI1 gene, lgi1a and lgi1b. Knockdown of lgi1a results in a seizure-like hyperactivity

Background: Seizures are considered a clinical sign in dogs with internal hydrocephalus but are not found in recent studies. Seizure prevalence due to ventricular enlargement and the prevalence of postoperative seizures in animals is not

We documented seizures in 33 of 68 (48.5%) children with congenital hydrocephalus not associated with myelomeningocele. Mental retardation (MR) and CNS malformations correlated with seizure occurrence; age at shunt insertion and number of shunt revisions and infections were not significant variables

Catabolites of purine nucleotides were measured in the cerebrospinal fluid (CSF) of newborn infants with sepsis, seizures and hydrocephalus using isocratic reversed-phase HPLC. The inosine levels in the CSF of the infants with any of the illnesses were significantly higher when compared with the

A 17-year-old boy with meningomyelocele, hydrocephalus with functioning shunt, seizures, and severe depression was treated with electroconvulsive therapy. His depression and social-scholastic behavior improved; no side effects or sequelae were seen.

OBJECTIVE Megalencephaly (MEG) or enlarged brain occurs as a mild familial variant with normal brain structure, but otherwise is an uncommon human brain malformation that may be associated with significant developmental and neurological problems. It has been classified into anatomic and metabolic

We report two sibs with Angelman syndrome or an apparently new syndrome. In addition to severe mental retardation and seizures, clinical examination showed an ataxic and stiff legged gait, truncal hypotonia with hypertonia of the limbs, dysmorphic facial features (brachycephaly, large mouth, pointed