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207 Possible Causes for 3-4 Hz Spike and Multispike, Hearing Loss Initially Affects Mid and High Frequencies, Onset in Infancy - First Year of Life

  • 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: 3-4 Hz Spike and Multispike
  • Benign Adult Familial Myoclonic Epilepsy

    Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3-4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24.[reference.medscape.com] […] 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] 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
  • 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
  • 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] 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] The spasms may be subtle and may be isolated at onset, typically clustering later in the course.[emedicine.medscape.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]

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

    Childhood absence epilepsy with tonic–clonic seizures and electroencephalogram 34Hz spike and multispike–slow wave complexes: linkage to chromosome 8q24.[doi.org] 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] ) 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
  • Epilepsy

    Contemporary drug therapy fails to control epileptic seizures in some 30% of patients, resulting in the need to employ other measures when they appear practicable. A good deal of potentially relevant statistical detail is available regarding the outcomes of the available antiepileptic therapies, but its interpretation[…][dx.doi.org]

    Missing: Hearing Loss Initially Affects Mid and High Frequencies Onset in Infancy - First Year of Life
  • Generalized Clonic or Tonic-Clonic Seizures

    ‘Contrary to popular folk belief, nothing should be placed in the mouth during the seizure. Severe injury could occur.’ Generalized tonic clonic seizures (grand mal seizures) are the most common and best known type of generalized seizure. They begin with stiffening of the limbs (the tonic phase), followed by jerking[…][epilepsynw.org]

    Missing: Hearing Loss Initially Affects Mid and High Frequencies Onset in Infancy - First Year of Life
  • Juvenile Myoclonic Epilepsy

    Juvenile myoclonic epilepsy is a common form of epilepsy mainly characterized by myoclonic jerks, but affected individuals may also experience generalized tonic-clonic seizures and absence seizures. Symptom onset typically occurs around puberty and although the disease persists into adulthood, patients do respond[…][symptoma.com]

    Missing: Hearing Loss Initially Affects Mid and High Frequencies Onset in Infancy - First Year of Life
  • Idiopathic Generalized Epilepsy

    Tonic status epilepticus (TSE) in patients with idiopathic generalized epilepsy (IGE) is not well recognized. The objective of this study is to report episodes of TSE in patients with IGE. We retrospectively reviewed the clinical and EEG evaluation of three IGE patients who presented TSE. The three patients had mainly[…][ncbi.nlm.nih.gov]

    Missing: Hearing Loss Initially Affects Mid and High Frequencies Onset in Infancy - First Year of Life

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