What does CES mean in BRITISH MEDICINE
CES, or Cat Eye Syndrome, is a rare genetic disorder characterized by abnormal eye shape, missing ocular muscles and/or malformations of the optic nerves. People with this condition typically have an abnormally wide-set eyes and may also experience issues related to vision loss. Additionally, those with Cat Eye Syndrome can have extra chromosomal material on their 11th chromosome.
CES meaning in British Medicine in Medical
CES mostly used in an acronym British Medicine in Category Medical that means cat eye syndrome
Shorthand: CES,
Full Form: cat eye syndrome
For more information of "cat eye syndrome", see the section below.
Symptoms
The most obvious physical symptom of CES is the wide-set eyes. Other symptoms of CES can include hearing loss, heart problems, kidney problems, and psychological difficulties such as autism or learning disabilities. Additionally, those with this syndrome may experience complications such as seizures or chronic pain.
Causes
The cause of Cat Eye Syndrome is usually due to a random genetic mutation on chromosome 11 that results in an extra copy of genetic material being present during development in the womb (trisomy 11). This trisomy 11 can directly lead to the physical malformations associated with CES.
Diagnosis
If you suspect your child has Cat Eye Syndrome it is important to seek medical attention right away as early diagnosis and treatment are essential for managing the condition. A physician may perform a physical exam as well as imaging tests like X-rays or ultrasounds, karyotype testing, and chromosomal microarray analysis to properly diagnose CES.
Treatment
There is no cure for Cat Eye Syndrome but there are treatments available that can help manage the symptoms and improve quality of life for those affected by this condition. Treatment options vary depending on the individual's specific symptoms but generally involve vision correction surgery if needed, physical therapy to manage mobility issues, hearing aids if necessary, and medications to help address any associated discomfort from chronic pain or seizures.
Essential Questions and Answers on cat eye syndrome in "MEDICAL»BRITMEDICAL"
What is CATS?
CATS, or Cat Eye Syndrome, is a chromosomal disorder caused by the presence of an extra piece of chromosome 22. It is a rare genetic condition that is believed to occur in between 1 in 50,000 and 1 in 150,000 births.
How does CATS affect those born with it?
Babies born with Cat Eye Syndrome typically have unique facial features such as wide-set eyes and low-set ears. Other symptoms vary depending on the severity of the disorder but may include intellectual disabilities, developmental delays, congenital heart defects and vision problems.
What are some signs and symptoms of CATS?
Some signs and symptoms associated with Cat Eye Syndrome include hypertelorism (wide-set eyes), strabismus (crossed eyes) epicanthal folds (downward sloping inner corners of the eyes), low set ears and learning difficulties. Additionally, babies may also experience hearing loss, speech impairments, motor skill delays and cleft palate.
Is CATS hereditary?
Yes; while it is generally considered to be a random occurrence, Cat Eye Syndrome can be inherited from parents who carry a genetic mutation for the disorder. It has been found that parents who have one child with CATS have a 25% chance of having another affected child due to the inheritance pattern.
How is CATS Diagnosed?
After physical examination from an eye specialist or pediatrician to check for any physical abnormalities present in newborns or infants who might be affected by Cat Eye Syndrome, further tests will be needed for diagnosis purposes. This includes chromosomal tests such as karyotyping or fluorescent in situ hybridization (FISH).
Is there any treatment available for cats?
Unfortunately there is currently no cure for this disorder however various treatments can help manage its symptoms. This includes speech therapy to help improve communication skills; occupational therapy to assist with daily activities; vision correction surgeries; hormone replacement therapies; physical/mobility therapies; psychological evaluations and counselling; nutritional supplements; medications to control seizures etc.
What kind of lifestyle changes should be made by people living with CATS?
People living with Cat Eye Syndrome must make various lifestyle changes depending on their individual needs including regular checkups at the doctor's office for monitoring purposes; follow up appointments for vision tests; regular exercise programs tailored specifically for each individual' s needs; minimizing exposure to environmental pollutants etc.
Are there any support groups available for families affected by this disorder?
Yes! There are many support groups both online and offline dedicated to helping those affected by Cat Eye Syndrome including Support Group for Families Affected by Chromosome 22 Disorders (SGFACD); Rare Chromosome Disorder Support Group (RCDG); Genetic Alliance UK etc.
Final Words:
Cat Eye Syndrome is a rare genetic disorder that affects people in different ways depending on the individual. It is important for those who suspect their child may have this condition to get them checked out right away so that any associated conditions can be identified early and treated appropriately. With early diagnosis and treatment individuals living with this syndrome can hopefully enjoy improved quality of life down the road.
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