Home Contact Sitemap

eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease encephalopathy
Symptom C0036572|seizures
Sentences 82
PubMedID- 21293276 The clinical presentation is usually of severe encephalopathy with refractory seizures and rett syndrome (rtt)-like phenotype.
PubMedID- 19822402 Clustered subclinical seizures in a patient with acute encephalopathy with biphasic seizures and late reduced diffusion.
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- 24132547 Five cytokines and five chemokines were measured in serum and cerebrospinal fluid (csf) obtained from 12 hhv-6b-associated acute encephalopathy with biphasic seizures and late reduced diffusion patients and 19 control exanthem subitum (without complications) patients.
PubMedID- 26571073 Purpose: the characteristics of electrographic seizures in newborns with hypoxic-ischaemic encephalopathy (hie) treated with therapeutic hypothermia (th) are poorly described.
PubMedID- 21792306 More recently, rufinamide was evaluated for the adjunctive treatment of childhood-onset epileptic encephalopathies and epileptic syndromes other than lgs, including epileptic spasms, multifocal epileptic encephalopathy with spasm/tonic seizures, myoclonic-astatic epilepsy, dravet syndrome and malignant migrating partial seizures in infancy.
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- 24842259 This represents one of the few documented examples of acute encephalopathy with biphasic seizures and late reduced diffusion in an individual not of east asian descent.
PubMedID- 20135578 Patient 1 who had mild mental retardation manifested acute encephalopathy with partial seizures and hemiplegia, mimicking encephalitis.
PubMedID- 24215384 Acute encephalopathy is manifested with seizures and coma, with or without multi-organ involvement.
PubMedID- 21459625 Subacute encephalopathy with seizures in chronic alcoholism (sesa) was first described in 1981 by niedermeyer who reported alcoholic patients presenting with confusion, seizures and focal neurological deficits and is quite distinct from patients presenting with typical alcohol withdrawal seizures.
PubMedID- 24969073 She subsequently developed seizures due to posterior reversible encephalopathy syndrome and required ongoing haemodialysis for oliguric aki.
PubMedID- 21937175 Acute encephalopathy with biphasic seizures and reduced diffusion (aesd) encompasses a group of encephalopathy characterized by biphasic seizures and disturbance of consciousness in the acute stage followed in the subacute stage by reduced diffusion in the subcortical white matter on magnetic resonance imaging.
PubMedID- 22240828 Background: dravet syndrome is a severe, genetic epileptic encephalopathy with seizures starting during the first year of life.
PubMedID- 25690439 Long-term risk of seizures and epilepsy in patients with posterior reversible encephalopathy syndrome.
PubMedID- 26118313 Objective: the aim of this study was to clarify characteristics of post-encephalopathic epilepsy (pee) in children after acute encephalopathy with biphasic seizures and late reduced diffusion (aesd), paying particular attention to precise diagnosis of seizure types.
PubMedID- 24411946 Two cases of traumatic head injury mimicking acute encephalopathy with biphasic seizures and late reduced diffusion.
PubMedID- 26242200 Prediction of acute encephalopathy with biphasic seizures and late reduced diffusion in patients with febrile status epilepticus.
PubMedID- 21883688 Background: acute encephalopathy with biphasic seizures and late reduced diffusion (aesd) is characterized clinically by biphasic seizures and late magnetic resonance imaging abnormalities, such as reduced subcortical diffusion from day 3 onwards, often accompanied with some neurological sequelae.
PubMedID- 24198884 It is a diffuse encephalopathy associated with seizures in at least 80% and status epilepticus, in up to a third of cases .
PubMedID- 26298309 Disrupted glutamate-glutamine cycle in acute encephalopathy with biphasic seizures and late reduced diffusion.
PubMedID- 24452957 Newborn babies with neonatal encephalopathy as a cause of seizures tend to have a higher seizure burden than those with a stroke .
PubMedID- 23248701 3 the clinical presentation ranges from a subtle illness to a fulminant encephalopathy with seizures, coma, and death.
PubMedID- 25008803 We divided the patients into two groups: acute encephalopathy with biphasic seizures and late reduced diffusion (aesd) and other encephalopathies.
PubMedID- 23853086 Hypoxic-ischaemic encephalopathy as the cause of gelastic-dacrystic seizures has not been reported so far in the literature.
PubMedID- 23772250 Acute encephalopathy with biphasic seizures and reduced diffusion (aesd) is a syndrome of encephalopathy characterized by biphasic seizures and altered consciousness in the acute stage followed in the subacute stage by restricted diffusion in the subcortical white matter on magnetic resonance imaging.
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- 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- 26333951 Acute encephalopathy with biphasic seizures and late reduced diffusion (aesd) at onset manifests an early seizure (es) usually lasting more than 30min.
PubMedID- 26005637 seizures of patients with epileptic encephalopathies are often resistant to antiepileptic drug therapies, but may respond to a ketogenic diet.
PubMedID- 24768152 Subacute encephalopathy with seizures in alcoholics (sesa) syndrome is a unique disease entity characterized by typical clinical and electroencephalographic (eeg) features in the setting of chronic alcoholism.
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- 19766516 Alpers disease, a neurodegenerative disease usually presents in the first years of life as a progressive encephalopathy with multifocal myoclonic seizures, developmental regression, cortical blindness and early death.
PubMedID- 24618220 Purpose: the aim of this paper is to describe two additional cases of subacute encephalopathy with seizures in alcoholics (sesa syndrome), and to propose that this entity now should be considered as a subtype of nonconvulsive status epilepticus (ncse).
PubMedID- 24324832 Therefore, the researchers concluded that mutations in szt2 can cause a severe type of autosomal recessive infantile encephalopathy with intractable seizures and distinct neuroradiological anomalies.
PubMedID- 21924570 Among syndromes of acute encephalopathy, acute encephalopathy with biphasic seizures and late reduced diffusion (aesd) was the most frequent, followed by clinically mild encephalitis/encephalopathy with a reversible splenial lesion (mers), acute necrotizing encephalopathy (ane) and hemorrhagic shock and encephalopathy syndrome (hses).
PubMedID- 23419470 Acute encephalopathy with biphasic seizures and late reduced diffusion was recently established clinicoradiologically as an encephalopathy syndrome.
PubMedID- 24516335 Melas is a mitochondrial syndrome defined by the clinical features of mitochondrial encephalopathy with dementia or seizures, and stroke-like episodes in individuals less than 40 years of age, myopathy with ragged red fibers on muscle biopsy, and lactic acidosis.10 melas is due to mutations of the mitochondrial genome and therefore follows a maternal inheritance pattern.
PubMedID- 23254984 Standard phenobarbital dosing is appropriate for the initial treatment of seizures in neonates with hypoxic ischemic encephalopathy treated with therapeutic hypothermia.
PubMedID- 23808377 Prolonged seizures were associated with acute encephalopathy in three scn1a mutation-positive patients.
PubMedID- 23008735 Ischemic stroke, hemorrhages, and a progressive encephalopathy with or without seizures may occur 4.
PubMedID- 22626713 Chronic progressive encephalopathy, intractable seizures, and neuropathy: a triad of neurological features in insulinoma.
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- 24550774 Ohtahara syndrome is the earliest appearing age-related epileptic encephalopathy with seizures first presenting as early as the neonatal period and is diagnosed with a characteristic burst-suppression pattern on eeg (yamatogi and ohtahara, 2002).
PubMedID- PMC4043902 Next 3 weeks she was relatively stabile, but became coushing-oid with occasional fever and high blood pressure, in the fourth week of hospitalization she developed seizures due to hypertensive encephalopathy (ta 210/160 mmhg).
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- 21331165 This disorder is thought to be similar to hypertensive encephalopathy and is associated with seizures, headaches, encephalopathy, and reversible imaging features.
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- 24384640 Pmes should be distinguished from progressive encephalopathies with seizures (due to degenerative conditions such as gm2 gangliosidosis, nonketotic hyperglycinemia, niemann-pick type c, juvenile huntington and alzheimer disease) and progressive myoclonic ataxias, which affect predominantly adults with progressive ataxia, myoclonus, few if any tonic-clonic seizures, and without evidence of dementia.(2,3.) rochester, mn.
PubMedID- 23379293 Background: anti-nmda-encephalitis is caused by antibodies against the n-methyl-d-aspartate receptor (nmdar) and characterized by a severe encephalopathy with psychosis, epileptic seizures and autonomic disturbances.

Page: 1 2