Goldenhar syndrome
(Redirected from Goldenhar Syndrome)
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Goldenhar syndrome | |
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Synonyms | Oculo-auriculo-vertebral spectrum (OAVS), hemifacial microsomia |
Pronounce | |
Specialty | N/A |
Symptoms | Facial asymmetry, ear abnormalities, eye abnormalities, spinal deformities |
Complications | Hearing loss, vision problems, breathing difficulties |
Onset | Congenital |
Duration | Lifelong |
Types | N/A |
Causes | Unknown, possibly genetic and environmental factors |
Risks | |
Diagnosis | Clinical examination, imaging studies |
Differential diagnosis | Treacher Collins syndrome, Nager syndrome |
Prevention | |
Treatment | Surgical intervention, hearing aids, speech therapy |
Medication | |
Prognosis | Variable, depends on severity |
Frequency | 1 in 3,500 to 1 in 5,600 live births |
Deaths |
Goldenhar Syndrome
Goldenhar Syndrome, also known as Oculo-Auriculo-Vertebral (OAV) syndrome, is a rare congenital condition characterized by the incomplete development or absence of facial structures, primarily affecting one side of the face.
Introduction
Goldenhar Syndrome is a birth defect that leads to abnormalities in the structure of the face. Affected individuals may have partially formed or absent ears, nose, lip, mandible (lower jaw), and/or soft palate. The condition can vary in severity and can be associated with other health issues.
Etiology
The exact cause of Goldenhar Syndrome is not fully understood, but it is believed to be a combination of genetic and environmental factors. There is no known single cause, and the condition occurs sporadically.
Clinical Features
Facial Abnormalities
Facial abnormalities in Goldenhar Syndrome can include underdeveloped facial muscles, a partially formed or absent external ear (microtia), and underdevelopment of the mandible (micrognathia).
Ocular Abnormalities
Ocular abnormalities may include coloboma (a defect in the eye structure), microphthalmia (small eyes), and anophthalmia (absence of one or both eyes).
Vertebral Abnormalities
Vertebral abnormalities such as scoliosis (curvature of the spine) and hemivertebrae (abnormally shaped vertebrae) are also common.
Diagnosis
Diagnosis of Goldenhar Syndrome is typically made based on physical examination and may be confirmed with imaging studies such as X-rays or MRI.
Treatment
Treatment for Goldenhar Syndrome is multidisciplinary and may involve surgical intervention, speech therapy, orthodontic treatment, and other supportive therapies depending on the individual's needs.
Prognosis
The prognosis for individuals with Goldenhar Syndrome varies depending on the severity of the condition and associated complications. Many individuals lead full, productive lives with appropriate medical and surgical management.
Resources and Support
Support for individuals and families affected by Goldenhar Syndrome is available through organizations like the Goldenhar Syndrome Association and other support groups.
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Contributors: Kondreddy Naveen, Prab R. Tumpati, MD