With the present sample size, we did not detect any significant differences in the types of auditory symptoms in families with vs without. Additional investigation of auditory symptom types with a larger sample size is warranted. [ncbi.nlm.nih.gov]

• Epilepsy

  Symbol definitions: □ ○ = Unaffected; ▪A •A = Idiopathic partial epilepsy with auditory features; ⊡ ⋅ = Unaffected mutation carrier; ▥ ◍ = Idiopathic generalized epilepsy; ◨ ◑ = Idiopathic partial and generalized epilepsy. [ncbi.nlm.nih.gov]

• Aura

  Table Clinical features in three newly identified ADPEAF families with LGI1 mutations Family Patient Age at onset Seizure type(s); and syndrome, if any* EEG findings (source) Auditory aura(s) Other aura(s) F II:1 10 SP, SGTC Left frontal-temporal transients [ncbi.nlm.nih.gov]

  Kobayashi E, Santos NF, Torres FR, Secolin R, Sardinha LA, Lopez-Cendes I, Cendes F (2003) Magnetic resonance imaging abnormalities in familial temporal lobe epilepsy with auditory auras. Arch Neurol 60(11):1546–1551 Article PubMed Google Scholar 4. [link.springer.com]

• Generalized Tonic-Clonic Seizure

  The remaining affected subject (IV:6) had two nocturnal generalized tonic-clonic seizures (GTCs) at age 10 and 11 years. No myoclonic or absence seizures were noted. [ncbi.nlm.nih.gov]

• Febrile Seizures

  Seizures precipitated by acute alterations in homeostasis or insults to the CNS (including febrile seizures) were excluded from the definition of epilepsy and classified as acute symptomatic. [ncbi.nlm.nih.gov]

• Receptive Aphasia

  volume changes), cognitive (receptive aphasia), and reflex (seizures precipitated by sounds; see supplementary data, classification of auditory symptoms and tables E1 to E3, on the Neurology Web site for additional details; go to www.neurology.org) [ncbi.nlm.nih.gov]

• Alteration of Consciousness

  He also described occasional eyelid twitching with these episodes and had no alteration of consciousness or confusion during or after these events. [ncbi.nlm.nih.gov]

This family illustrates that rare epilepsy syndromes within a single family can have both genetic and structural etiologies. [link.springer.com]

These frequently contained additional seizure descriptions, histories of etiologic factors, and EEG and neuroimaging data. Some patients were also given a brief neurologic examination and a study EEG. [ncbi.nlm.nih.gov]