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200 Possible Causes for Onset of Deafness in Early Childhood

  • Perrault Syndrome Type 2

    SNHL is bilateral and ranges from profound with prelingual ( congenital ) onset to moderate with early-childhood onset.[ncbi.nlm.nih.gov] Of note, the variable age of onset and degree of deafness do not depend on the sex of the affected individual.[ncbi.nlm.nih.gov]

  • Deafness - Opticoacoustic Nerve Atrophy - Dementia Syndrome

    Definition An X-linked recessive disorder characterized by postlingual sensorineural deafness with onset in early childhood, dystonia, spasticity, dysphagia, mental deterioration[uniprot.org] Acronym MTS Synonyms DDS DFN-1 Dystonia-deafness syndrome Jensen syndrome Opticoacoustic nerve atrophy with dementia X-linked progressive deafness type 1 Keywords Disclaimer[uniprot.org]

  • Usher Syndrome Type I

    People with Usher type 1 develop profound deafness from birth and in early childhood symptoms of RP become evident.[retina-international.org] People with Usher type 1 develop profound deafness from birth and early childhood symptoms of RP.[fightingblindness.ie] The deafness is generally so early in onset and so severe that hearing aids may not be of value, (although cochlear implants may be beneficial), and patients fail to develop[retina-international.org]

  • Usher Syndrome, Type 3

    People with Usher type 1 develop profound deafness from birth and early childhood symptoms of RP.[fightingblindness.ie] The deafness is generally so early in onset and so severe that hearing aids may not be of value, (although cochlear implants may be beneficial), and patients fail to develop[fightingblindness.ie]

  • Usher Syndrome Type 3B

    People with Usher type 1 develop profound deafness from birth and early childhood symptoms of RP.[fightingblindness.ie] The deafness is generally so early in onset and so severe that hearing aids may not be of value, (although cochlear implants may be beneficial), and patients fail to develop[fightingblindness.ie]

  • Usher Syndrome Type 1J

    People with Usher type 1 develop profound deafness from birth and early childhood symptoms of RP.[fightingblindness.ie] The deafness is generally so early in onset and so severe that hearing aids may not be of value, (although cochlear implants may be beneficial), and patients fail to develop[fightingblindness.ie]

  • Usher Syndrome Type 2

    People with Usher type 1 develop profound deafness from birth and early childhood symptoms of RP.[fightingblindness.ie] The deafness is generally so early in onset and so severe that hearing aids may not be of value, (although cochlear implants may be beneficial), and patients fail to develop[fightingblindness.ie]

  • Brown-Vialetto-Van Laere Syndrome

    Format Definition An autosomal recessive progressive neurologic disorder characterized by early childhood onset of sensorineural deafness, bulbar dysfunction, and severe diffuse[uniprot.org] Confusing it is possible to have presentations without the deafness, in which case the presentation has the phenotype of childhood bulbar motor neuron disease ( Fazio-Londe[ganfyd.org] childhood-onset nystagmus Early childhood-onset sensory (gait) ataxia Childhood onset sensorineural deafness Weakness and atrophy of the upper limbs (first distally then[ncbi.nlm.nih.gov]

  • Wolfram Syndrome

    The onset of symptoms in Wolfram syndrome almost universally occurs in childhood and early adolescence.[symptoma.com] Clinical Presentation: Early childhood in onset IDDM and vision loss are the first and essential features of WFS, followed by development of deafness, diabetes insipidus,[ajnr.org] […] mellitus, diabetes insipidus, optic atrophy, and deafness, which is why the term DIDMOAD is sometimes used in the literature.[symptoma.com]

  • CK Syndrome

    An X-linked recessive neuromuscular disorder characterized by early childhood onset of a slowly progressive axonal sensorimotor neuropathy associated in some patients with[nectarmutation.org] […] sensorineural deafness and cognitive impairment. [ read more ] 23217327 FKBP10 causing BRKS1 259450 The disease is caused by mutations affecting the gene represented in this[nectarmutation.org]

Further symptoms