PedAM

Pediatric Disease Annotations & Medicines

Disease	encephalopathy
Symptom	\|seizures
Sentences	84
PubMedID- 24411946	Acute encephalopathy with biphasic seizures and late reduced diffusion (aesd) presents a distinct clinical course of biphasic seizures and impaired consciousness.
PubMedID- 22626713	Chronic progressive encephalopathy, intractable seizures, and neuropathy: a triad of neurological features in insulinoma.
PubMedID- 21603166	seizures, altered levels of consciousness and encephalopathy, focal neurologic deficits and diffuse neurologic symptoms (headache, nausea, and vomiting) may result; presentation with pseudotumor cerebri and isolated headache has also been documented .
PubMedID- 25008803	We divided the patients into two groups: acute encephalopathy with biphasic seizures and late reduced diffusion (aesd) and other encephalopathies.
PubMedID- 19896902	Infants born after 36 or more completed weeks' gestation who showed signs of moderate or severe encephalopathy, with or without seizures, were assessed with amplitude integrated eeg.12 infants were randomly assigned, by central telephone randomisation within 6 h of birth, to a control group (rectal temperature kept to within 0·2°c of 37°c) or to whole-body cooling (rectal temperature kept at 33–34°c for 72 h).
PubMedID- 26242200	Prediction of acute encephalopathy with biphasic seizures and late reduced diffusion in patients with febrile status epilepticus.
PubMedID- 26333951	Predictive score for early diagnosis of acute encephalopathy with biphasic seizures and late reduced diffusion (aesd).
PubMedID- 23865558	These include, but are not limited to parkinsonism, chronic progressive external ophthalmoplegia (cpeo), cerebellar ataxia, sensory polyneuropathy, alpers-huttenlocher syndrome, which is characterized by progressive encephalopathy with seizures and hepatic failure, isolated myoclonic epilepsy or non-syndromic liver failure.
PubMedID- 24418041	Background: acute encephalopathy with biphasic seizures and late reduced diffusion (aesd) is the most common syndrome among the acute encephalopathies, and is associated with a high incidence of neurologic sequelae.
PubMedID- 19822402	Clustered subclinical seizures in a patient with acute encephalopathy with biphasic seizures and late reduced diffusion.
PubMedID- 25336011	Many studies have reported acute encephalopathy with biphasic seizures and late reduced diffusion (aesd) associated with viral infection at onset, but few studies have reported aesd without infection.
PubMedID- 19556082	Acute encephalopathy with biphasic seizures and late reduced diffusion associated with hemophagocytic syndrome.
PubMedID- 23808377	Prolonged seizures were associated with acute encephalopathy in three scn1a mutation-positive patients.
PubMedID- 25690439	Long-term risk of seizures and epilepsy in patients with posterior reversible encephalopathy syndrome.
PubMedID- 19679415	Acute encephalopathy with biphasic seizures and late reduced diffusion (aesd) is a recently clinicoradiologically-established encephalopathy syndrome.
PubMedID- 21666586	Cases with epileptiform eeg-changes, which are not associated with epileptic seizures and clinical signs of epileptic encephalopathy, are frequent in practical child neurology.
PubMedID- 23240532	Acute encephalopathy with biphasic seizures and late reduced diffusion (aesd) is characterized by biphasic clinical course and high intensity of subcortical white matter in mri diffusion images appearing around the late seizure.
PubMedID- 23848569	Key findings: ceeg indications were encephalopathy with possible seizures in 67% of subjects, event characterization in 38% of subjects, and management of refractory status epilepticus in 11% of subjects.
PubMedID- 25944474	Fifty-three showed photoparoxysmal response and were diagnosed as having dravet syndrome (11), epileptic encephalopathy with myoclonic seizures (8), neurodegenerative disorders (8), benign idiopathic epilepsies (9), and static disorders with a known or suspected genetic origin (17).
PubMedID- 24115962	The clinical diagnosis of melas is based on the following features: 1) stroke-like episodes occurring before the age of 40, 2) encephalopathy with seizures and/or dementia, 3) the presence of lactic acidosis, ragged red muscle fibres, as well as additional criteria such as recurrent headaches and recurrent vomiting.
PubMedID- 23248701	3 the clinical presentation ranges from a subtle illness to a fulminant encephalopathy with seizures, coma, and death.
PubMedID- 22577545	In one study seizures occurred in 25% of children, encephalopathy in 25%, facial palsy in 12%, and hemiplegia in 8% .
PubMedID- 23254984	Standard phenobarbital dosing is appropriate for the initial treatment of seizures in neonates with hypoxic ischemic encephalopathy treated with therapeutic hypothermia.
PubMedID- 23755112	Rois: regions of interest, aesd: acute encephalopathy with biphasic seizures and late reduced diffusion, ane: acute necrotizing encephalopathy, uc: uncategorizable.
PubMedID- 22474467	A case of hashimoto's encephalopathy presenting with seizures and psychosis.
PubMedID- 24768152	A pathophysiologic approach for subacute encephalopathy with seizures in alcoholics (sesa) syndrome.
PubMedID- 26571073	Purpose: the characteristics of electrographic seizures in newborns with hypoxic-ischaemic encephalopathy (hie) treated with therapeutic hypothermia (th) are poorly described.
PubMedID- 25340058	Case 2 (f, age 10) presented 3 weeks after first symptoms when her encephalopathy worsened with intractable seizures, movement disorder, and hyperpyrexia.
PubMedID- 25941511	A rare syndrome of fulminant encephalopathy with manifestations of seizures, bradykinesia, myoclonia, and bilateral mri hyperintensities in basal ganglia has been described in hiv-positive cocaine abusers (152).
PubMedID- 23535492	Objective: acute encephalopathy with biphasic seizures and late reduced diffusion (aesd) is a childhood encephalopathy following severe febrile seizures, leaving neurologic sequelae in many patients.
PubMedID- 21399511	Continuous spike and waves during sleep is an age-related epileptic encephalopathy that presents with neurocognitive regression, seizures, and an eeg pattern of electrical status epilepticus during sleep.
PubMedID- 26005637	Ohtahara syndrome is one form of early infantile epileptic encephalopathy with medically intractable seizures and progressive neurodevelopmental deterioration.
PubMedID- 26314768	Human parechovirus type 3 (hpev-3) is a neurotropic virus which can cause neonatal encephalitis, presenting as encephalopathy with seizures and diffuse white matter lesions on brain imaging.
PubMedID- 20816272	There are distinct clinical features for nmt (cramps, stiffness, fasciculations, myokymia, hyperhidrosis; afterdischarges and continuous motor activity on electromyogram), le (encephalopathy with seizures, deficient recent memory; hyponatremia, temporal lobe magnetic resonance imaging and electroencephalographic abnormalities) and mvs (nmt plus hyperhidrosis, dysautonomia, encephalopathy, severe insomnia, and sleep disorders).

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