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643 Possible Causes for Epilepsy, Exotropia

  • Narcolepsy

    Abstract We report a 5-year-old boy with epilepsy and narcolepsy-cataplexy.[] Narcolepsy type 1 and focal epilepsy was diagnosed.[] Four patients with comorbidity for narcolepsy type 1 and idiopathic generalized epilepsy are reported: in three cases the onset of epilepsy preceded narcolepsy type 1 appearance[]

  • Cataplexy

    Cataplexy is a strange neurologic condition, occasionally confused with epilepsy.[] Cataplexy is also sometimes confused with epilepsy, where a series of flashes or other stimulus cause similar seizures.[] Cataplexy mimics include syncope, epilepsy, hyperekplexia, drop attacks and pseudocataplexy.[]

  • Congenital Toxoplasmosis

    Microencephaly, intellectual disability, vision impairment, hydrocephalus, and epilepsy are common outcomes of congenital toxoplasmosis.[] A nine-week-old Caucasian male presented with right ptosis and right exotropia due to a third cranial nerve palsy.[] Meta-analysis of three case controlled studies and an ecological study into the link between cryptogenic epilepsy and chronic toxoplasmosis infection.[]

  • Sturge-Weber Syndrome

    A 15-year-old boy with Sturge-Weber syndrome underwent strabismus surgery (oculus sinister [OS]) for the treatment of exotropia.[] Thirteen did not develop epilepsy. Patients with bilateral port-wine stain were at higher risk of epilepsy (P 0.03).[] BACKGROUND: Sturge-Weber syndrome (SWS) is strongly associated with epilepsy.[]

  • Familial Porencephaly

    CPK Increased creatine kinase Increased creatine phosphokinase Increased serum CK Increased serum creatine kinase Increased serum creatine phosphokinase [ more ] 0003236 Exotropia[] Abnormal Cortical Development and Epilepsy . London : John Libbey , pp. 181 –9.[] Neuroimaging in investigation of patients with epilepsy. Continuum (Minneap Minn) . 2013 Jun. 19(3 Epilepsy):623-42. [Medline] . Kim H, Mansi T, Bernasconi N.[]

  • Antidepressant Toxicity

    A few examples are: Hyperserotonemia , such as the lifethreatening condition the Serotonin Syndrome , Epileptiform Discharges, Epileptic Seizures and/or Epilepsy , Hypoglycaemia[] This also "explains the high rates of epilepsy in autism: because of BDNF release, the brain maps are poorly differentiated, and because so many connections in the brain have[] Tumours & Bleedings Go to: Hepato Toxicity (Liver Damage) Go to: Cardiovascular Toxicity (Heart Damage) & Neurological Toxicity (Brain Damage) Go to: Epileptiform Activity, Epilepsy[]

  • Generalized Clonic or Tonic-Clonic Seizures

    Thoracic hypoplasia Cerebellar atrophy Femoral bowing Delayed skeletal maturation Sleep apnea Tibial bowing Rhizomelia Hypertrophic cardiomyopathy Wide anterior fontanel Exotropia[] Other Generalised Epilepsies, such as Juvenile Myoclonic Epilepsy and Juvenile Absence Epilepsy , which share the same propensity to GTCS on awakening.[] 1 Dynamic functional network connectivity in idiopathic generalized epilepsy with generalized tonic-clonic seizure. ( 27726245 ) Liu F....Chen H. 2017 2 Valproate in adolescents[]

  • Facial Hemiatrophy

    Parry-Romberg syndrome presenting with recurrent exotropia and torticollis. J Pediatr Ophthalmol Strabismus. 2008 Nov-Dec;45(6):368-70.[] We report four patients with PFH associated with partial epilepsy in whom brain MRI showed cerebral dysgenesis.[] The cranial CT and MRI appearances of a 14-year-old girl with Parry-Romberg syndrome and epilepsy are described.[]

  • Congenital Non-Progressive Ataxia

    We herein report a case of atypical Gillespie syndrome associated with bilateral ptosis, exotropia, corectopia, iris hypoplasia, anterior capsular lens opacities, foveal hypoplasia[] […] lobe epilepsy Benign familial neonatal epilepsy Benign familial neonatal-infantile seizures Benign hereditary chorea Benign infantile focal epilepsy with midline spikes and[] Case report: We herein report a case of atypical Gillespie syndrome associated with bilateral ptosis, exotropia, corectopia, iris hypoplasia, anterior capsular lens opacities[]

  • Kohlschütter-Tönz Syndrome

    Protruding ear Gastroesophageal reflux Glaucoma Reduced visual acuity Amblyopia Retinal detachment Opacification of the corneal stroma Recurrent urinary tract infections Exotropia[] TY - JOUR T1 - Kohlschütter-Tönz syndrome: epilepsy, dementia, and amelogenesis imperfecta.[] American Journal of Medical Genetics 46453-454 (1993) Kohlschtter-Tonz Syndrome: Epilepsy, Dementia, and Amelogenesis Imperfecta Joel Zlotogora, Anna Fuks, Zvi Borochowitz[]

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