About Keratitis-Ichthyosis-Deafness Syndrome

Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant, also known as kid syndrome, is related to keratitis, hereditary and nonsyndromic hearing loss and deafness, dfnb1, and has symptoms including photophobia An important gene associated with Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant is GJB2 (Gap Junction Protein Beta 2), and among its related pathways/superpathways are G-protein signaling G-Protein alpha-i signaling cascades and Myometrial relaxation and contraction pathways. Affiliated tissues include skin, eye and tongue, and related phenotypes are corneal neovascularization and abnormality of the dentition

Major Symptoms of Keratitis-Ichthyosis-Deafness Syndrome

Keratitis-ichthyosis-deafness syndrome is a rare genetic disorder that affects the eyes, skin, and hearing. The major symptoms include dry and irritated eyes, itchy, scaling skin on the face, and hearing loss.

Suitable Lifestyle for People with Keratitis-Ichthyosis-Deafness Syndrome

Suitable lifestyle options for people with Keratitis-ichthyosis-deafness syndrome include:

1. Avoid exposure to the sun to reduce eye irritation.

2. Avoid using irritating eye drops to avoid aggravating symptoms.

3. Perform regular eye massage to relieve symptoms.

4. Avoid smoking and prolonged use of electronic products to reduce eye irritation.

5. Maintain good living habits, including adequate sleep, a balanced diet and moderate exercise.

6. If the symptoms are severe, you may consider wearing a hearing aid or avoiding prolonged exposure to noisy environments to reduce stimulation to the hearing system.

7. Have regular physical exams to ensure you are in good health.

Other Diseases

Keratitis Sensorineural Deafness Sudden Deafness Neurological Deafness Ichthyosis Neurogenic Tinnitus and Deafness X-Linked Ichthyosis Lamellar Ichthyosis Congenital and Acquired Profound Deafness Maternally Inherited Diabetes and Deafness

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