What does AOA mean in PEDIATRIC
Ataxia with oculomotor apraxia (AOA) is a rare, genetic disorder characterized by movement difficulties and poor eye control. It is caused by a mutation in theSETX gene, which is located on chromosome 3. AOA affects individuals from infancy to adulthood and symptoms can range from mild to severe.
AOA meaning in Pediatric in Medical
AOA mostly used in an acronym Pediatric in Category Medical that means Ataxia with oculomotor apraxia
Shorthand: AOA,
Full Form: Ataxia with oculomotor apraxia
For more information of "Ataxia with oculomotor apraxia", see the section below.
Essential Questions and Answers on Ataxia with oculomotor apraxia in "MEDICAL»PEDIATRIC"
What is Ataxia with Oculomotor Apraxia?
Ataxia with oculomotor apraxia (AOA) is a rare, genetic disorder characterized by movement difficulties and poor eye control.
What causes AOA?
AOA is caused by a mutation in the SETX gene, which is located on chromosome 3.
Who does AOA affect?
AOA affects individuals from infancy to adulthood and can range from mild to severe.
What are the symptoms of AOA?
Symptoms of AOA include difficulty walking or maintaining balance, poor coordination when performing tasks requiring fine motor skills, involuntary jerking movements (myoclonus), loss of muscle strength, tremors, hearing and vision problems, dementia, learning disabilities and delayed speech development.
Is there any treatment for AOA?
There is currently no cure for AOA but medications may be used to help manage some of its symptoms such as seizures or muscle spasms. Physical therapy may also help improve mobility and coordination skills as well as social skills.
Final Words:
Ataxia with oculomotor apraxia (AOA) is a rare disorder that has no known cure yet but treatments can help alleviate some of its symptoms allowing those affected to lead a more comfortable life.
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