PedAM
Pediatric Disease Annotations & Medicines
| Disease | encephalopathy |
| Symptom | C0036572|seizures |
| Sentences | 84 |
| PubMedID- 25439110 | A missed diagnosis: acute encephalopathy with biphasic seizures and late reduced diffusion. |
| 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- 24215384 | Acute encephalopathy is manifested with seizures and coma, with or without multi-organ involvement. |
| PubMedID- 26298309 | Disrupted glutamate-glutamine cycle in acute encephalopathy with biphasic seizures and late reduced diffusion. |
| 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- 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- 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- 26118313 | Seizure characteristics of epilepsy in childhood after acute encephalopathy with biphasic seizures and late reduced diffusion. |
| 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- 26316206 | Potential breed-specific diseases that may mimic idiopathic epilepsy: for the standard poodle, a neonatal encephalopathy with seizures (news) has been reported that may play a role as potential differential in standard poodle puppies with 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- 26311622 | Objective: acute encephalopathy with biphasic seizures and late reduced diffusion (aesd) is a childhood encephalopathy following severe febrile seizures. |
| PubMedID- 26566404 | The baby developed grade 3 hypoxic-ischemic encephalopathy (hie) with seizures and underwent therapeutic hypothermia (head cooling) and was discharged several days later with very guarded long-term prognosis. |
| PubMedID- 21800694 | Acute encephalopathy with biphasic seizures and late reduced diffusion with visual disturbance and higher brain dysfunction. |
| PubMedID- 24842259 | Conclusions: this presentation is reminiscent of acute encephalopathy with biphasic seizures and late reduced diffusion, a syndrome thus far reported almost exclusively in japan. |
| 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- 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. |
| 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- 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- 23401780 | In a melanoma patient, an inflammatory encephalopathy picture with seizures, stupor, signs of meningeal irritation, nausea, moderate increase in temperature took place starting 24 hours after intraventricular administration of 50 mg of liposomal arac; concomitantly, a slight intraventricular csf lymphocytosis was detected. |
| 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- 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- 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- 23269594 | The typical clinical picture consisted of recurrent subacute encephalopathy leading to coma, seizures, and extrapyramidal manifestations. |
| PubMedID- 23853086 | Hypoxic-ischaemic encephalopathy as the cause of gelastic-dacrystic seizures has not been reported so far in the literature. |
| 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- 21293276 | The clinical presentation is usually of severe encephalopathy with refractory seizures and rett syndrome (rtt)-like phenotype. |
| 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- 22240828 | Background: dravet syndrome is a severe, genetic epileptic encephalopathy with seizures starting during the first year of life. |
| PubMedID- 21941682 | The condition may present as a subacute or acute encephalopathy with seizures, stroke-like episodes, myoclonus, and tremor . |
| 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- 23419470 | The combination regimen of dextromethorphan and cyclosporine a could be effective for the treatment and prevention of acute encephalopathy with biphasic seizures and late reduced diffusion. |
| PubMedID- 25193414 | Thalamic lesions in acute encephalopathy with biphasic seizures and late reduced diffusion. |
| 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- 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- 23772250 | Acute encephalopathy with biphasic seizures and late reduced diffusion. |
| 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- 20979196 | Homozygous loss of chrna7 on chromosome 15q13.3 causes severe encephalopathy with seizures and hypotonia. |
| 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- 21331165 | This disorder is thought to be similar to hypertensive encephalopathy and is associated with seizures, headaches, encephalopathy, and reversible imaging features. |
| PubMedID- PMC2934076 | seizures accounted for 38% of patients and hepatic encephalopathy in two. |
| 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- 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- 20135578 | Patient 1 who had mild mental retardation manifested acute encephalopathy with partial seizures and hemiplegia, mimicking encephalitis. |
| 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- 24452957 | Newborn babies with neonatal encephalopathy as a cause of seizures tend to have a higher seizure burden than those with a stroke . |
| PubMedID- 24969073 | She subsequently developed seizures due to posterior reversible encephalopathy syndrome and required ongoing haemodialysis for oliguric aki. |
| 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- 24075506 | Serum and cerebrospinal fluid levels of visinin-like protein-1 in acute encephalopathy with biphasic seizures and late reduced diffusion. |
| PubMedID- 23008735 | Ischemic stroke, hemorrhages, and a progressive encephalopathy with or without seizures may occur 4. |
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