Create issue ticket

305 Possible Causes for Onset of Hearing Loss in Childhood

  • Metabolic Syndrome

    […] with insulin resistance, acanthosis nigricans, hyperlipidemia, childhood progressive retinal degeneration or retinitis pigmentosa and neurosensory hearing loss or deafness[] Alstrom syndrome (ALMS) is a very rare genetic autosomal recessive disease, characterized by early-onset severe abdominal obesity, impaired glucose tolerance or type 2 diabetes[]

  • Presbycusis

    High risk factors for delayed, late-onset and/or progressive hearing loss.[] Cochlear implantation for progressive hearing loss.(Short Report). Archives of Disease in Childhood 88.8 (August 2003): p708(4).[] Beyond Newborn Hearing Screening: Recognizing the Signs of Late Onset Hearing Loss in Infants and Young Children. Boys Town National Research Hospital. .[]

  • Deafness

    Additionally, we observed severe speech disorder in two young family members with the onset of hearing loss began in their early childhood.[]

  • Pallidopyramidal Syndrome

    LOSS; CAPOS Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss (CAPOS) is an autosomal dominant neurologic disorder characterized by early-childhood[] onset of recurrent episodes of acute ataxic encephalopathy associated with febrile illnesses.[] ORPHANET OMIM MONDO More info about SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE; SPG78 Medium match CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURAL HEARING[]

  • Migrainous Stroke

    Sensorineuronal hearing loss is common.[] It is a multisystem disease, with age at onset in childhood with generalised tonic-clonic seizures and migraine-like episodes with headache, vegetative symptoms and abdominal[]

  • Sudden Hearing Loss

    […] of the loss.[] Many childhood diseases and common viral infections can lead to sudden hearing loss.[] However, most cases of sudden hearing loss occurs as a result of infections, especially viral infections.[]

  • Eye Muscle Disorder

    When FSHD starts in childhood, loss of hearing in the higher pitch ranges can be more profound than in adult-onset FSHD. The reason for this isn't yet understood.[] The reason for the hearing loss, when it occurs, isn’t clear.[]

  • Long QT Syndrome

    One autosomal recessive subtype of LQTS, Jervell and Lange-Nielsen syndrome ( JLNS ), is characterized by congenital bilateral sensorineural hearing loss as well as early-onset[] (childhood) cardiac arrhythmias and a very prolonged QTc interval.[]

  • Leukoerythroblastic Anemia

    loss; psychomotor retardation Childhood Poor TABLE 1 Three Variants of Osteopetrosis Variant Inheritance pattern Pathophysiology Clinical features Age of onset Prognosis[] Marble bone disease Autosomal recessive Abnormal osteoclastic bone resorption No bone marrow failure; renal tubular acidosis; intracranial calcifications; sensorineural hearing[]

  • Wolfram Syndrome

    […] diabetes mellitus, optic nerve atrophy and vision loss, diabetes insipidus, and hearing impairment.[] […] understanding these less well-known symptoms of WFS. 1 Introduction Wolfram syndrome (WFS) [ 1 ], is a rare, autosomal recessive neurodegenerative disorder characterized by childhood-onset[]

Further symptoms