Mondini dysplasia
Mondini dysplasia is a rare congenital abnormality in the inner ear that can cause hearing loss and balance problems. It is named after the Italian anatomist Carlo Mondini, who first described it in 1791.
Symptoms[edit | edit source]
The main symptom of Mondini dysplasia is sensorineural hearing loss, which can range from mild to profound. This type of hearing loss is caused by damage to the cochlea, the part of the inner ear that converts sound vibrations into nerve signals. Other symptoms can include vertigo, tinnitus, and a feeling of fullness in the ear.
Causes[edit | edit source]
Mondini dysplasia is caused by an incomplete development of the cochlea during the early stages of embryonic development. The exact cause of this abnormal development is not known, but it is thought to be due to a combination of genetic and environmental factors.
Diagnosis[edit | edit source]
The diagnosis of Mondini dysplasia is usually made through a combination of audiometry (hearing tests) and imaging studies such as MRI or CT scan. These tests can show the characteristic abnormalities of the cochlea that are seen in this condition.
Treatment[edit | edit source]
There is no cure for Mondini dysplasia, but the symptoms can be managed with hearing aids or cochlear implants. In some cases, surgery may be needed to correct the structural abnormalities of the inner ear.
See also[edit | edit source]
References[edit | edit source]
Mondini dysplasia Resources | |
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Contributors: Prab R. Tumpati, MD