Similar Diseases
- DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA
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- Autosomal recessive sensorineural hearing impairment, dizziness, and hypodontia
- Autosomal dominant deafness 1
- Cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss
- Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features
- Autosomal dominant deafness 13
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- SFMMP
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Results for Query ‹ DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA medication ›
Michel aplasia – Prevention of secondary complications | Surveillance
This can be done by annual evaluations by multidiciplinary team involving otolaryngologist, clinical geneticist, a pediatrician, the expertise of an educator of the deaf, a neurologist is appropriate.
Michel aplasia – Prevention of secondary complications
Presence of inner ear abnormalities lead to Delayed gross development of child because of balance impairment and profound deafness which increases the risk of trauma and accidents.
- Incidence of accidents can be decreased by using visual or vibrotactile alarm systems in homes as well as in schools.
- Anticipatory education of parents, health providers and educational programs about hazards can help.