Microtia
Microtia is a congenital condition in which the external ear (pinna) is underdeveloped or entirely absent. Most commonly affecting one ear—usually the right—it occurs in approximately one out of every 8,000 to 10,000 births. In some cases, microtia may be associated with hearing loss due to the absence or malformation of the ear canal, and it may present as part of a broader syndrome such as Treacher-Collins or Goldenhar syndrome.
Grades
Grade I: slightly small ear, identifiable structures present
Grade II: partial ear, canal narrowing or absence
Grade III: most common – small vestigial lobule or “peanut,” no canal/tunnel
Grade IV (anotia): complete absence of external ear
Surgical Process and Recovery
Ear reconstruction is a multi-stage process involving meticulous planning and execution. The first stage typically involves the creation and placement of the ear framework. In cartilage reconstruction, additional stages refine the ear’s shape and position. If hearing restoration is indicated, surgery may include canal reconstruction or the placement of a BAHA implant. Dr. Jarrahy’s extensive experience ensures optimal surgical outcomes and minimal complications. Postoperative care includes regular follow-up visits, wound management, and monitoring of hearing function.