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      <video:title>Aural-Atresia</video:title>
      <video:description>Congenital aural atresia is a common congenital ear deformity in children. It arises from abnormal development of the first branchial cleft during embryonic growth, resulting in partial or complete closure of the external auditory canal.

Most cases are accompanied by auricular hypoplasia and middle ear structural anomalies, restricting the development of auditory ossicles. Clinically, conductive hearing loss of varying severity occurs on the affected side, which may impair language development in severe cases. Complications such as middle ear cholesteatoma may also occur.

Absent or abnormal ear canals can usually be detected at birth. Definitive diagnosis relies on high-resolution CT to identify bony or cartilaginous atresia and evaluate middle ear bone development, combined with pure-tone audiometry to assess hearing impairment severity.

For mild atresia, bone conduction hearing aids are initially prescribed to improve hearing. Severe cases require external auditory canal reconstruction surgery to reopen the canal and restore sound conduction. Surgical procedures involve removing atretic bone and soft tissue, expanding or reconstructing the ear canal, and repairing the tympanic membrane and ossicles. Regular postoperative cleaning is essential to prevent stenosis and recurrent infection.

Adopting advanced international microsurgery techniques and auxiliary bone conduction devices, Dr. Kesser has helped numerous children regain hearing after surgery. Potential surgical risks include facial nerve injury, recurrent stenosis and otitis media, requiring long-term follow-up by specialized medical teams.</video:description>
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