Goldenhar syndrome is a rare congenital condition characterized by abnormal development of the eye, ear and spine. Children with Goldenhar syndrome are born with partially formed or totally absent …

Goldenhar syndrome is a rare congenital defect characterized by incomplete development of the ear, nose, soft palate, lip and mandible on usually one side of the body.

Goldenhar syndrome is a rare disorder that’s present at birth. It’s a craniofacial condition, meaning it affects the development of your face and skull. Most babies with the condition have hemifacial …

Sep 10, 2025 · What is Goldenhar syndrome? Goldenharsyndrome is a rarecongenital condition characterized by abnormal development of the face, ears, and vertebrae.

Feb 14, 2024 · Learn what Goldenhar syndrome is, how it affects your body, and the available treatment options.

Goldenhar syndrome (oculo-auriculo-vertebral dysplasia, OAVS) is a rare, congenital disease arising from the abnormal development of the first and second branchial arches.

Mar 27, 2014 · What Is Goldenhar Syndrome? Goldenhar syndrome, also known as oculo-auriculo-vertebral spectrum or hemifacial microsomia, is a rare congenital disorder featuring abnormal …

Oct 20, 2022 · Genetic and environmental factors may play a role in the development of these disorders. In this article, we will explore what Goldenhar syndrome is, what causes it, and its symptoms and...

Some babies are born with a condition called Goldenhar syndrome. It can cause incomplete development of bones in the face, affecting the ears, nose, soft palate, lips, and jaw. Usually, this …

Learn about Goldenhar Syndrome, a congenital craniofacial condition affecting one side of the face, its features, treatment considerations, and support resources from FACES