Rett syndrome is a rare genetic disorder that affects brain development, resulting in severe mental and physical disability.
It is estimated to affect about 1 in 12,000 girls born each year and is only rarely seen in boys.
Some children with Rett syndrome are affected more severely than others. Also, the age at which symptoms first appear varies from child to child.
A child may not have all the symptoms of Rett syndrome and their symptoms might change as they get older.
Rett syndrome is described in 4 stages, although symptoms will often overlap between each stage. These are the main features of each stage:
Stage 1: early signs
At first, the child will appear to develop and grow normally for at least 6 months. There may be subtle signs of Rett syndrome before the child is recognised as having a problem (especially with hindsight).
Stage 1 is sometimes described as "stagnation". Symptoms include:
- low muscle tone (hypotonia)
- difficulty feeding
- unusual, repetitive hand movements or jerky limb movements
- delay with development of speech
- mobility problems, such as problems sitting, crawling and walking
- lack of interest in toys
These symptoms typically begin from 6 to 18 months and often last for several months, although they can persist for a year or more.
Stage 1 can often go unnoticed because the changes occur gradually and may be subtle.
Stage 2: regression
During stage 2, known as "regression" or the "rapid destructive stage", the child starts to lose some of their abilities. This stage usually begins between the ages of 1 and 4 and may last for any time from 2 months to more than 2 years.
The child will gradually or suddenly start to develop severe problems with communication and language, memory, mobility, co-ordination and other brain functions. Some of the characteristics and behaviours are similar to those of autism.
Signs at this stage include:
- loss of the ability to use the hands purposefully – repetitive hand movements are often difficult to control and include wringing, washing, clapping or tapping
- periods of distress, irritability and sometimes screaming for no obvious reason
- social withdrawal – a loss of interest in people and avoidance of eye contact
- unsteadiness and awkwardness when walking
- problems sleeping
- slowing of head growth
- difficulty eating, chewing or swallowing, and sometimes constipation that may cause tummy aches
Later on during regression, the child may experience periods of rapid breathing (hyperventilation) or slow breathing, including breath-holding. They may also swallow air which can lead to abdominal bloating.
Stage 3: plateau
Stage 3 of Rett syndrome can begin as early as 2 years or as late as 10 years. It often lasts for many years, with many children remaining in this stage for most of their lives.
During stage 3, some of the stage 2 symptoms may get better – for example, there may be improvements in behaviour, with less irritability and crying.
The child may become more interested in people and their surroundings, and there may be improvements in alertness, attention span and communication. Their walking may also improve (or they may learn to walk, if they could not before).
Other symptoms at this stage include:
- seizures, which may become more common
- irregular breathing patterns may get worse – for example, shallow breathing followed by rapid, deep breathing, or breath holding
Gaining and maintaining weight can also be difficult to achieve.
Stage 4: deterioration in movement
Stage 4 can last for years or even decades. The main symptoms at this stage are:
- development of a spinal curve (the spine bending to the left or right side), known as scoliosis
- muscle weakness and spasticity (abnormal stiffness, particularly in the legs)
- losing the ability to walk
Communication, language skills and brain function do not tend to get any worse during stage 4. The repetitive hand movements may decrease and eye gaze usually improves.
Seizures also usually become less of a problem during teenage and early adult life, although they will often be a lifelong problem to manage.
Almost all cases of Rett syndrome are caused by a mutation (a change in the DNA) in the MECP2 gene, which is found on the X chromosome (one of the sex chromosomes).
The MECP2 gene contains instructions for producing a particular protein (MeCP2), which is needed for brain development. The gene abnormality prevents nerve cells in the brain from working properly.
There's usually no family history of Rett syndrome, which means it is not passed on from one generation to the next. Almost all cases (over 99%) are spontaneous, with the mutation occurring randomly.
Rett syndrome is usually diagnosed based on your child's symptoms, and by ruling out other more common disorders.
A diagnosis of Rett syndrome may not be made for a number of years because the syndrome is so rare and symptoms do not tend to appear until a child is between 6 and 18 months old.
A genetic blood test can be used to identify if the genetic mutation is responsible for Rett syndrome. If a change is found in the MECP2 gene, it can help confirm the diagnosis, but failing to find it does not necessarily rule out the syndrome.
Read more about genetic testing.
There's no cure for Rett syndrome, so treatment focuses on managing the symptoms.
As a parent caring for a child with the syndrome, it's likely you'll need help and support from a wide range of healthcare professionals.
Your child may benefit from some of the following treatments and aids:
- speech and language therapy, picture boards, eye gaze technology and other visual aids to help with communication
- medication for breathing and mobility problems, and anti-epileptic medicine to control seizures
- physiotherapy, attention to mobility, careful attention to your child's sitting posture (to minimise the chances of scoliosis developing), and frequent changes in posture
- if scoliosis does become established, a back brace and sometimes spinal surgery may be used to prevent the spine curving further (read more about treating scoliosis)
- a high-calorie diet to help maintain sufficient weight, with the use of a feeding tube and other feeding aids if necessary
- occupational therapy to help develop the skills needed for dressing, feeding and other daily activities
- an ankle-foot orthosis (lower leg brace) to help them walk independently
- a hand splint to help control hand movements, if these are severe (they're mainly used for limited periods to prevent self-injury or to encourage activities with the other hand)
- beta blocker medicine or a pacemaker to control their heart rhythm
Therapeutic horse riding, swimming, hydrotherapy and music therapy have also been reported to be beneficial. Ask your healthcare team where you can access these therapies.
Although some people with Rett syndrome may retain a degree of hand control, walking ability and communication skills, most will be dependent on 24-hour care throughout their lives.
Many people with Rett syndrome reach adulthood, and those who are less severely affected can live into old age. However, some people die at a fairly young age as a result of complications, such as heart rhythm abnormalities, pneumonia and epilepsy.
Caring for a child with Rett syndrome is mentally and physically challenging. Most carers will need social and psychological support.
Your guide to care and support provides lots of information and advice about how you can take time to look after yourself, including:
You may also find it useful to contact a support group, such as Rett UK, for information and advice about looking after a child with the syndrome.
If your child has Rett syndrome, your clinical team will pass information about them on to the National Congenital Anomaly and Rare Diseases Registration Service (NCARDRS).
This helps scientists look for better ways to treat and prevent the syndrome. You can opt out of the register at any time.