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260 Possible Causes for Hearing Loss Initially Affects Mid and High Frequencies, Onset in Infancy - First Year of Life, Slowing with Polyspike-and-Slow-Waves

  • Autosomal Recessive Deafness 103

    الصفحة 296 - Embryonic stem cells develop into functional dopaminergic neurons after transplantation in a Parkinson rat model. ‏ الصفحة 108 - Mutation in mitochondrial tRNAIeu (UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness. Nat. Genet. ‏ الصفحة 312 - Lumelsky, N.,[…][books.google.com]

    Missing: Slowing with Polyspike-and-Slow-Waves
  • Benign Adult Familial Myoclonic Epilepsy

    […] in 6 to 7% of children with seizure onset in the first year of life 90 and is a severe form of epilepsy, characterized by multiple seizure types and unfavorable prognostic[clinicalgate.com] […] or polyspike and slow-wave complexes.  Variable course and outcome.  One half experience encephalopathic effects and suffer from persistent GTCS, myoclonic-atonic status[slideshare.net] Epileptic Syndromes with Secondarily Generalized Epileptic Myoclonus Severe Myoclonic Epilepsy in Infancy (SMEI), or Dravet Syndrome SMEI, or Dravet syndrome, is observed[clinicalgate.com]

    Missing: Hearing Loss Initially Affects Mid and High Frequencies
  • Myoclonic-Astatic Epilepsy

    Myoclonic status in nonprogressive encephalopathies This rarely reported disorder has onset in infancy or early childhood, with onset usually during the first year of life[emedicine.medscape.com] Atonia is usually concurrent with the slow wave of a single- or polyspike-wave complex.[medlink.com] Malignant epilepsy with migrating partial seizures in infancy Onset of this rare syndrome occurs in the first year of life, in some cases in the neonatal period.[emedicine.medscape.com]

    Missing: Hearing Loss Initially Affects Mid and High Frequencies
  • West Syndrome

    West syndrome: Infantile spasms, a seizure disorder of infancy and early childhood with the onset predominantly in the first year of life of myoclonic seizures, hypsarrhythmia[medicinenet.com]

    Missing: Hearing Loss Initially Affects Mid and High Frequencies
  • Progressive Myoclonic Epilepsy Type 8

    […] in 6 to 7% of children with seizure onset in the first year of life 90 and is a severe form of epilepsy, characterized by multiple seizure types and unfavorable prognostic[clinicalgate.com] […] fast spikes, polyspikes and polyspike‐and‐wave discharges Slow background activity, spike‐ and polyspike‐and‐wave discharges and multifocal spikes activated by non‐REM sleep[onlinelibrary.wiley.com] Epileptic Syndromes with Secondarily Generalized Epileptic Myoclonus Severe Myoclonic Epilepsy in Infancy (SMEI), or Dravet Syndrome SMEI, or Dravet syndrome, is observed[clinicalgate.com]

    Missing: Hearing Loss Initially Affects Mid and High Frequencies
  • Early Infantile Epileptic Encephalopathy Type 3

    Severe Myoclonic Epilepsy in Infancy or Dravet Syndrome is a severe form of EE with the following features: Onset is commonly during the first year of life Seizure types include[centogene.com] […] paroxysms of polyspikes or spikes-slow waves.  Ictal EEG  Varies according to seizure type. 16.[slideshare.net] .  Inter-Ictal EEG  Initial -20% show normal BG with photoparoxysmal discharges of spikes/ polyspikes-slow waves.  Within 1 year, EEG - abnormal slow BG with frequent asymmetrical[slideshare.net]

    Missing: Hearing Loss Initially Affects Mid and High Frequencies
  • Familial Infantile Myoclonic Epilepsy

    3 years of life ( Dravet and Bureau 1981 ).[medlink.com] […] or polyspike and slow-wave complexes.  Variable course and outcome.  One half experience encephalopathic effects and suffer from persistent GTCS, myoclonic-atonic status[slideshare.net] Severe Myoclonic Epilepsy in Infancy or Dravet Syndrome is a severe form of EE with the following features: Onset is commonly during the first year of life Seizure types include[centogene.com]

    Missing: Hearing Loss Initially Affects Mid and High Frequencies
  • Hypoglycemia

    An 84-year-old Japanese woman with metastatic insulinoma suffered from frequent hypoglycemic events. Continuous glucose monitoring (CGM) confirmed severe and frequent symptomatic/asymptomatic hypoglycemia. After the initiation of everolimus treatment, the hypoglycemic events were rapidly eliminated. CGM revealed[…][ncbi.nlm.nih.gov]

    Missing: Hearing Loss Initially Affects Mid and High Frequencies Onset in Infancy - First Year of Life
  • Benign Familial Infantile Epilepsy Type 4

    Severe Myoclonic Epilepsy in Infancy or Dravet Syndrome is a severe form of EE with the following features: Onset is commonly during the first year of life Seizure types include[centogene.com] […] background Irregular generalized spike or polyspike and slow wave complexes Photosensitive, decreased during sleep Prognosis: Slow progression, may live to 60s Lafora Disease[emilytam.com] 6 years of life are benign myoclonic epilepsy of infancy.[emedicine.medscape.com]

    Missing: Hearing Loss Initially Affects Mid and High Frequencies
  • Generalized Epilepsy with Febrile Seizures Plus

    SCN1A mutations occur also in severe myoclonic epilepsy of infancy (SMEI), a rare convulsive disorder characterized by febrile seizures with onset during the first year of[doi.org] EEG recordings showed a variety of changes: generalized spike wave and polyspike wave activity, focal discharges, focal or diffuse slowing or were normal.[brain.oxfordjournals.org] ) is a rare epilepsy syndrome with seizure onset in the first year of life often triggered by fever, infectious diseases, or vaccinations in a previously healthy child.[pediatrics.aappublications.org]

    Missing: Hearing Loss Initially Affects Mid and High Frequencies