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Inner ear disorder
- Ménière disease is a disorder of the inner ear that affects balance and hearing. This condition is characterized by sudden episodes of extreme dizziness (vertigo), a roaring sound in ...
- ... loss of hearing caused by abnormalities in the inner ear. Other features of the disorder include weak muscle tone (hypotonia), impaired muscle coordination ( ...
- ... loss, which is caused by abnormalities of the inner ear. Fibrochondrogenesis appears to be a rare disorder. About 20 affected individuals have been described in ...
- ... and young adulthood, and gradually gets worse. An inner ear abnormality affecting both ears occurs in most people with this disorder. This feature, which is called enlarged vestibular aqueduct, ...
- ... profound hearing loss caused by changes in the inner ears (sensorineural deafness). Developmental delay and intellectual disability are also often severe in this disorder.The nail abnormalities affect both the hands and ...
- ... hearing loss caused by nerve damage in the inner ear (sensorineural hearing loss) may be present. Intelligence is usually not affected.As the disorder worsens, the muscles that control breathing become weakened ...
- ... aplasia, microtia, and microdontia National Organization for Rare Disorders (NORD) DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA PubMed Alsmadi O, Meyer ...
- ... develop hearing loss caused by abnormalities of the inner ear (sensorineural ... disorder develop renal disease, usually beginning in early adulthood. ...
- ... insipidus), hearing loss caused by changes in the inner ear (sensorineural deafness), urinary tract problems, reduced amounts of the sex hormone testosterone in males (hypogonadism), or neurological or psychiatric disorders.Diabetes mellitus is typically the first symptom of ...
- ... the mutation are limited to cells in the inner ear and the skin in this condition. GJB2 MT-TS1 Palmoplantar keratoderma with deafness can have different inheritance patterns.When this disorder is caused by GJB2 gene mutations, it is ...