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191 Possible Causes for 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]

  • Streptococcal Infection

    About 12,000 of the 3.5 million babies born in the United States each year develop GBS disease in infancy. About 75% of them develop early-onset infection.[medical-dictionary.thefreedictionary.com] About 12,000 of the 3.5 million babies born in the United States each year develop GBS disease in infancy. About 75 percent of them develop early-onset infection.[healthofchildren.com] Sometimes evident within a few hours of birth and always apparent within the first week of life, this condition causes inflammation of the membranes covering the brain and[medical-dictionary.thefreedictionary.com]

    Missing: Hearing Loss Initially Affects Mid and High Frequencies
  • Atopic Dermatitis

    What you should be alert for in the history Onset occurs in the first year of life in approximately 60% of patients, with most developing signs and symptoms between the third[clinicaladvisor.com] Atopic dermatitis (AD) is a chronic, relapsing, pruritic dermatosis that commonly presents in early infancy or childhood.[clinicaladvisor.com]

    Missing: Hearing Loss Initially Affects Mid and High Frequencies
  • Moraxella Catarrhalis

    Onset in first year of life Onset in infancy [ more ] 0003593 Leukocytosis Elevated white blood count High white blood count Increased blood leukocyte number [ more ] 0001974[rarediseases.info.nih.gov] […] mouth Abnormal mouth 0000153 Abnormality of the skin 0000951 Autosomal dominant inheritance 0000006 Hearing impairment Deafness Hearing defect [ more ] 0000365 Infantile onset[rarediseases.info.nih.gov]

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

    3 years of life ( Dravet and Bureau 1981 ).[medlink.com] 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] ) 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
  • 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] ) 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] […] by febrile seizures with onset during the first year of life, followed by intractable epilepsy, impaired psychomotor development, and ataxia ( Dravet and Bureau, 1981 ; Scheffer[doi.org]

    Missing: Hearing Loss Initially Affects Mid and High Frequencies
  • 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] 6 years of life are benign myoclonic epilepsy of infancy.[emedicine.medscape.com] Age of onset is usually between 4 months and 3 years. [6] However, as reported by Rossi et al, later onset up to 4 years and 8 months is possible. [7] Genetics The genetics[emedicine.medscape.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] 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
  • 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] 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

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