Goldenhar Syndrome 1 | Movahed OMS

Condition

Goldenhar Syndrome

Goldenhar Syndrome, also known as oculo-auriculo-vertebral spectrum, is a rare congenital disorder characterized by facial and craniofacial abnormalities. It typically involves underdevelopment of the ear, resulting in hearing loss, as well as jaw and facial asymmetry, eye abnormalities, and spinal defects. Other associated features may include cleft lip or palate, heart defects, and kidney abnormalities. The condition varies in severity.

Common Symptoms

Facial asymmetry, with one side of the face appearing smaller or underdeveloped. Ear abnormalities, such as microtia or hearing loss, are often present. Eye abnormalities, including ptosis, coloboma, or anisocoria, may also be observed. Jaw abnormalities, such as micrognathia or retrognathia, can affect the lower jaw. Other features can include spinal defects like scoliosis, cleft lip or palate, heart defects, and kidney abnormalities. It’s important to remember that the specific combination and severity of symptoms can vary among individuals with Goldenhar syndrome.