How long do people with Goldenhar syndrome live?
How long do people with Goldenhar syndrome live?
It’s a craniofacial condition, meaning it affects the development of your face and skull. Most babies with the condition have hemifacial microsomia and underdeveloped bones and muscles in one side of their face. With treatment, most children with Goldenhar syndrome live a relatively normal lifespan.
Can people with Goldenhar syndrome have kids?
That means if one parent has Goldenhar syndrome, each of their children has a 50 percent chance of inheriting the disorder. However, for most individuals with Goldenhar syndrome, the chance of them having a child with the disorder is very low.
Can Goldenhar syndrome be cured?
Goldenhar syndrome cannot be cured. Treatment is focused on helping people live their best life possible with the disease. This can include speech therapy, treatments to address feeding difficulties, hearing and vision problems, heart surgery, ear reconstruction, and jaw surgery.
Is Goldenhar syndrome a disability?
Approximately 15% of individuals with Goldenhar syndrome have an intellectual disability. The likelihood for an intellectual disability increases if the individual has microphthalmia. Heart defects and kidney defects can also occur with Goldenhar syndrome.
Does Goldenhar syndrome affect the brain?
Goldenhar syndrome may also affect the face and other body organs, such as heart, kidney, lungs and nervous system (the brain, spinal cord and nerves working together). In most cases, the deformity only affects one side of the body.
Can Goldenhar syndrome be seen on ultrasound?
Conclusions: Goldenhar syndrome is a rare abnormality which could be diagnosed prenatally using non-invasive imaging methods as ultrasound scan and MRI.
Can you detect Goldenhar syndrome before birth?
Goldenhar syndrome is a rare birth defect with unknown aetiology. Prenatal suspicion is possible but no genetic diagnosis is yet available. The prognosis depends on the presented malformations and association with systemic defects. Multidisciplinary evaluation is essential to reach this challenging clinical diagnosis.
Is Goldenhar syndrome rare?
Goldenhar syndrome is a rare disorder that affects the formation of the skull, head, and face. The syndrome is congenital, which means it is present at birth. Another name for this disorder is oculoauriculovertebral dysplasia. Goldenhar syndrome affects one out of every 3,500 to 25,000 children at their time of birth.
How is Goldenhar syndrome treated?
Treatments for Goldenhar syndrome In some mild cases, no treatment is needed. Children may need to work with a hearing specialist or speech therapist for hearing issues, or may need a hearing aid. If there are vision problems, corrective surgery or glasses may be needed.
What causes Goldenhar syndrome?
Causes of Goldenhar syndrome Goldenhar syndrome is a congenital disease, meaning that it is present in infants when they are born. The cause is an abnormality in a chromosome. It is usually not inherited. In about 1 or 2 percent of cases, though, the condition is inherited as a genetic disorder.