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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease encephalopathy
Symptom |seizures
Sentences 82
PubMedID- PMC2934076 seizures accounted for 38% of patients and hepatic encephalopathy in two.
PubMedID- 25439110 A missed diagnosis: acute encephalopathy with biphasic seizures and late reduced diffusion.
PubMedID- 20507773 encephalopathy with generalized seizures and loss of consciousness preceded death in both cases.
PubMedID- 25313971 Computed tomography in new-onset status epilepticus, as well as high rates of identification of electrographic seizures in patients with unexplained acute encephalopathy in pediatric icu settings.
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- 22871019 Since february 2006, the second generation tyrosine-kinase inhibitor (tki) dasatinib induced a hematological remission (chronic phase) until a one antigen mismatched (c-allele locus) unrelated allogeneic hematopoietic stem cell transplantation (sct) was performed in may 2006. after sct, she developed a series of epileptic seizures owing to posterior reversible encephalopathy syndrome (pres) and developed severe critical illness polyneuropathy.
PubMedID- 25193414 Thalamic lesions in acute encephalopathy with biphasic seizures and late reduced diffusion.
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- 26109926 Clinical observations in our tbm patient group include the classical profile of encephalopathy with manifestations of seizures, involuntary movements, fever, impaired consciousness, poor feeding and vomiting, indicative of neuroinflammatory responses and impaired neuronal functioning (udani and dastur 1970).
PubMedID- 24075506 Background: acute encephalopathy with biphasic seizures and late reduced diffusion (aesd) has recently been recognized as an encephalopathy subtype.
PubMedID- 23932106 We conclude that mutations in szt2 cause a severe type of autosomal-recessive infantile encephalopathy with intractable seizures and distinct neuroradiological anomalies.
PubMedID- 21941682 The condition may present as a subacute or acute encephalopathy with seizures, stroke-like episodes, myoclonus, and tremor .
PubMedID- 22620018 Acute encephalopathy with biphasic seizures and late reduced diffusion (aesd) is characterized clinically by biphasic seizures and late mri abnormalities such as reduced subcortical diffusion.
PubMedID- 25156649 Background: theophylline has recently been suspected as a risk factor of acute encephalopathy with biphasic seizures and late reduced diffusion (aesd), although there has been no systematic study on the relationship between acute encephalopathy in children taking theophylline (aet) and aesd.
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- 22577545 In one study seizures occurred in 25% of children, encephalopathy in 25%, facial palsy in 12%, and hemiplegia in 8% .
PubMedID- 22474467 A case of hashimoto's encephalopathy presenting with seizures and psychosis.
PubMedID- 20979196 Homozygous loss of chrna7 on chromosome 15q13.3 causes severe encephalopathy with seizures and hypotonia.
PubMedID- 19556082 Acute encephalopathy with biphasic seizures and late reduced diffusion associated with hemophagocytic syndrome.
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- 22571747 Main outcome measures: neonatal encephalopathy with seizures and/or death, encephalopathy within 24 hours of birth, 5-minute apgar scores and neonatal unit admission.
PubMedID- 26212315 Patient description: we report a 1-month-old boy manifesting an epileptic encephalopathy with clonic seizures refractory to phenobarbital, pyridoxine and phenytoin that presented a dramatic response to levetiracetam with full epilepsy control and eeg normalization.
PubMedID- 26311622 Objective: acute encephalopathy with biphasic seizures and late reduced diffusion (aesd) is a childhood encephalopathy following severe febrile seizures.
PubMedID- 22958032 Hypothermia may decrease seizures in newborns with encephalopathy and a focal infarct, potentially improving the long-term outcome for these infants.
PubMedID- 21800694 Acute encephalopathy with biphasic seizures and late reduced diffusion (aesd) is a recently described clinicoradiologic syndrome.
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).
PubMedID- 23981388 Conclusions: a significantly increased thalamic volume may be provide an objective imaging measure for predicting seizures due to minimal hepatic encephalopathy in cirrhotic patients.
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- 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- 23269594 The typical clinical picture consisted of recurrent subacute encephalopathy leading to coma, seizures, and extrapyramidal manifestations.
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- 19679415 Acute encephalopathy with biphasic seizures and late reduced diffusion (aesd) is a recently clinicoradiologically-established encephalopathy syndrome.

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