aural atresia, congenital

Aural atresia, congenital is a rare condition that is present at birth and affects the development of the ear. The name of the condition suggests that it involves underdevelopment or absence of the ear canal. It is also known by other names such as CAA and aural atresia, congenital, with hyposmia. Detailed clinical descriptions and definitions are currently limited for this condition.

Information about symptoms is currently limited for this condition.

There is a known association with the gene TSHZ1 in people with aural atresia, congenital. This suggests that changes in this gene may play a role in the development of the condition, though additional genetic or environmental factors have not been clearly established at this time.

Information about treatment options and management is currently limited for this condition.

Information about prognosis and quality of life considerations is currently limited for this condition.

Information about current research and future directions is currently limited for this condition.