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Angelman syndrome is a genetic disorder that affects the nervous system and causes severe physical and intellectual disability.
It’s relatively rare, occurring in approximately 1 in 25,000 people.
Typical characteristics of Angelman syndrome include:
- delayed development (usually noticeable from 6-12 months of age)
- severe language impairment with little or no speech
- movement and balance problems (ataxia)
- frequent seizures (epilepsy) in around 85% of cases
- a small head size (microcephaly)
- sociable behaviour with frequent smiling
In most cases, Angelman syndrome isn’t inherited from your parents, and the genetic anomaly responsible for the syndrome occurs by chance around the time of conception. However, in some families, more than one child is affected (see below).
Characteristics of Angelman syndrome
The typical characteristics of Angelman syndrome aren’t usually apparent at birth.
A child with the syndrome will begin to show signs of delayed envelopment around 6-12 months, such as being unable to sit unsupported or make babbling noises. Later, they may not speak at all or may only be able to say a few words.
The movement of a child with Angelman syndrome will also be affected. They may have difficulty walking due to problems with balance and co-ordination (ataxia), their arms may tremble or move jerkily, and their legs may be stiffer than normal.
A number of distinctive behaviours are also associated with Angelman syndrome. These may include:
- frequent laughter and smiling, with little stimulus
- being easily excitable, often flapping the hands
- being restless (hyperactive)
- having a short attention span
- problems sleeping, needing less sleep than other children
By around two years of age, an abnormally small head that’s flat at the back (microbrachycephaly) will often be noticeable. They may also start to have seizures (fits) around this age.
Other possible features of the syndrome include:
- sticking the tongue out
- crossed eyes (strabismus)
- pale skin, and light-coloured hair and eyes
- a wide mouth with widely spaced teeth
- a side-to-side curvature of the spine (scoliosis)
- walking with arms in the air
- a fascination with water
Some young babies with Angelman syndrome may have problems feeding, because they’re unable to co-ordinate sucking and swallowing. In such cases, a high-calorie formula may be recommended to help the baby gain weight, or they may need to be treated for reflux.
What causes Angelman syndrome?
The typical characteristics of Angelman syndrome are caused when a gene, known as UBE3A, is either absent or malfunctions. A gene is a single unit of DNA.
A person usually inherits one copy of the UBE3A gene from each parent. Both copies are switched on (active) in most of the body’s tissues. However, in certain areas of the brain, only the gene inherited from the mother is active.
In most cases (about 70%), the child’s maternal copy of the UBE3A gene is missing, which means there’s no active copy of the UBE3A gene in the child’s brain.
In around 11% of cases, the maternal copy of the UBE3A gene is altered (mutation).
In a small number of cases, Angelman syndrome occurs when a child inherits two copies of chromosome 15 from the father, rather than inheriting one from each parent. It can also occur when the copy of the UBE3A gene that comes from the mother, behaves like it came from the father. This is known as an “imprinting defect”.
In about 10-15% of cases, the cause of Angelman syndrome is unknown. It’s thought that most children in these unexplained cases may have different conditions involving other genes or chromosomes.
Diagnosing Angelman syndrome
Angelman syndrome may be suspected if a child’s development is delayed and they have the distinctive characteristics of the syndrome (see above).
A blood sample can be taken to confirm the diagnosis. A number of genetic tests will be carried out on the sample. These may include:
- chromosome analysis – to see if any parts of the chromosomes are missing
- fluorescence in situ hybridisation (FISH) – used to check chromosome 15 deletions
- DNA methylation – shows whether the genetic material on both the mother’s and father’s chromosomes is active; it can detect deletions, uniparental disomy and imprinting defects
- UBE3A gene mutation analysis – if the results of DNA methylation are normal, UBE3A gene sequencing can see whether the maternal copy of the gene is altered
For each child with Angelman syndrome, it’s important to know the genetic change that caused the condition to determine the risk of it occurring again in another child.
Most children with Angelman syndrome are diagnosed between the ages of 18 months and 6 years, when the typical physical and behavioural symptoms become apparent.
If your child is diagnosed with Angelman syndrome, you should be given the opportunity to discuss the genetic diagnosis and implications with a genetic doctor.
Managing Angelman syndrome
There’s no cure for Angelman syndrome, because it’s not possible to alter the genes and chromosomes in the brain.
Some of the symptoms can be difficult to manage, and you’re likely to need help from a wide range of different health professionals.
Your child may benefit from some of the following treatments and aids:
- Anti-epileptic medicine to control the seizures – sodium valproate, clonazepam or ethosuximide may be prescribed.
- Physiotherapy may help to improve posture, balance and walking ability. It’s also important to prevent permanent stiffening (contractures) of the joints as they get older.
- Back brace or spinal surgery may be recommended to prevent the spine from becoming more curved (see treating scoliosis).
- An ankle foot orthosis (lower leg brace) to help them walk independently.
- Communication therapy to help them develop non-verbal language skills, such as sign language and using visual aids. Using iPad applications and similar devices may also help.
- Behavioural therapy to overcome problem behaviours, hyperactivity and a short attention span.
- Activities such as swimming, horseriding and music therapy have also been reported as beneficial.
Read more about caring for a disabled child.
With age, people with Angelman syndrome become less hyperactive and the sleeping problems tend to improve. Most people with the condition will have intellectual disability and limited speech throughout their life.
In later childhood, the seizures usually improve, although they may return in adulthood. In adults, some mobility may be lost and joints may stiffen up.
A person with Angelman syndrome will have a near-normal life expectancy, but will need looking after for the rest of their life.
As a parent carer, it’s important that you look after your own health and wellbeing too.
Read more about carers’ wellbeing.
- Published Date
- 2014-09-30 13:20:30Z
- Last Review Date
- 2014-09-01 00:00:00Z
- Next Review Date
- 2016-09-01 00:00:00Z
- Disability (living with)
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