Congenital absence of (ear) auricle digital illustration

Congenital absence of (ear) auricle Save


ICD-10 code: Q16.0

Disease category: Q16: Congenital malformations of ear causing impairment of hearing

Congenital Absence of Ear Auricle: Causes and Symptoms

Congenital absence of the ear auricle, also known as microtia, is a rare condition where a baby is born with a partially or completely undeveloped external ear. This condition can affect one or both ears and can vary in severity. While the exact cause of microtia is not fully understood, several factors are believed to contribute to its development.

  1. Genetic Factors: Microtia can be inherited from parents who carry certain genetic mutations. Studies have shown that certain genes play a role in ear development, and any alterations in these genes can result in microtia.
  2. Environmental Factors: Exposure to certain environmental factors during pregnancy, such as medications, infections, or chemical substances, may increase the risk of developing microtia. However, the specific triggers are not yet identified.
  3. Other Birth Defects: Microtia is sometimes associated with other congenital abnormalities, such as facial clefts or heart defects. These conditions may occur due to similar genetic or environmental factors.

Microtia can be classified into different grades based on the severity of the ear malformation. In grade 1 microtia, the ear is slightly smaller or misshapen but still has some structures. In grade 2 microtia, the ear is smaller and lacks some of the typical ear components. Grade 3 microtia involves a more significant absence of ear structures, leaving only a small remnant. In grade 4 microtia, the ear is completely absent.

Common symptoms of microtia include hearing loss in the affected ear, as well as aesthetic concerns due to the ear's deformity. The severity of hearing loss can vary, ranging from mild to complete deafness in the affected ear. It is important to note that microtia does not affect a person's intelligence or cognitive abilities.

Diagnosing microtia usually occurs shortly after birth when the ear abnormality is visible. Medical professionals can conduct further tests, such as hearing evaluations, to determine the extent of hearing loss if present. Early intervention is crucial to address any associated hearing difficulties and ensure appropriate support for the child's development.

While treatment options for microtia exist, it is important to consult with a healthcare professional to discuss the available options and make an informed decision. Treatment may involve reconstructive surgery to create a new ear using the patient's own tissue or a prosthetic ear.

In conclusion, congenital absence of the ear auricle, or microtia, is a condition where a baby is born with an underdeveloped external ear. Genetic and environmental factors are believed to contribute to its development

Treatment of Congenital absence of (ear) auricle:

Treatment Options for Congenital Absence of (Ear) Auricle

Congenital absence of the auricle, also known as microtia, is a rare condition where a child is born with a partially formed or missing external ear. This can lead to hearing difficulties and aesthetic concerns. Fortunately, there are several treatment options available to address this condition and improve the quality of li...

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