Noonan syndrome is a genetic disorder that causes a wide range of features which can vary from person to person.
The most common features of Noonan syndrome are:
The severity of these features can range from mild to life-threatening.
Read more about the symptoms of Noonan syndrome.
The condition is usually diagnosed at birth, although milder cases may go undiagnosed until a child gets older.
Noonan syndrome is relatively uncommon. It is estimated that around 1 in 2,500 children are born with it. It affects both sexes and all ethnic groups equally.
Read more about diagnosing Noonan syndrome.
Researchers have identified eight specific genetic mutations that cause Noonan syndrome. A genetic mutation happens when the normal instructions that are carried in certain genes become scrambled. This means that some of the body’s processes don't work in the normal way.
However, it is unclear exactly how these mutations cause all the symptoms associated with Noonan syndrome.
Read more about causes of Noonan syndrome.
There is currently no cure for Noonan syndrome, so treatment involves trying to manage the various symptoms and complications that can arise from the condition.
The outlook for children with Noonan syndrome depends on how serious their congenital heart disease is (if they have it - around 80-90% of children with Noonan syndrome do). Some types of congenital heart disease are mild and only require careful monitoring. Other types can be life-threatening and require immediate emergency surgery.
However, almost all children with congenital heart disease reach adulthood. Most adults with Noonan syndrome do not require specialist medical care but may benefit from occasional cardiac follow-up. They are usually able to lead full and independent lives.
Read more about treatment for Noonan syndrome.
Noonan syndrome can affect a person in many different ways. Not everyone with the disorder will share the same characteristics.
The three most common characteristics of Noonan syndrome are:
These are discussed in more detail below.
Unless your child is only mildly affected by Noonan's syndrome, facial features associated with the condition usually become apparent following birth.
As your child gets older, their face is likely to become more triangular. Their lips may also thicken and the folds of skin that run from each side of the nose to the corners of the mouth may become more noticeable.
By the time your child reaches their teenage years, their eyes will become less prominent and their neck should become longer. However, the lengthening of the neck can reveal extensive folds of skin (skin webbing). By adulthood, the eyelids will look thick and hooded.
Children with Noonan syndrome also have abnormalities that affect the bones of the chest such as:
Children born with Noonan syndrome are usually a normal length at birth. Their short stature usually becomes apparent when they are around two years old.
After this time, they don't grow as quickly as children of the same age. Puberty (when a child begins to mature sexually and physically) is typically delayed for up to two years and the expected growth spurt that happens during puberty is either reduced or doesn’t happen at all.
This is sometimes treated with a type of medication, known as human growth hormone. Left untreated, the average adult height for men with Noonan syndrome is 162.5cm (5ft 3in) and for women is 153cm (5ft).
Read more information about restricted growth.
An estimated 80-90% of children with Noonan syndrome will have some form of congenital heart disease. This may be one of the following:
Pulmonary stenosis is the most common type of congenital heart disease, affecting around half of all children with Noonan syndrome. It occurs when the pulmonary valve (the valve that helps control the flow of blood away from the heart and into the lungs) is unusually narrow. This means that the heart has to work much harder to pump blood into the lungs. In many cases there will be no symptoms and no treatment is required, but if the obstruction is severe it can be corrected by surgery (see below).
Hypertrophic cardiomyopathy (HCM) is the second most common type of congenital heart disease in children with Noonan syndrome, affecting an estimated 20-30% of children.
In cases of HCM, the muscles of the heart are much larger than they should be. This can place strain on the heart and cause symptoms such as breathlessness.
HCM in Noonan syndrome can cause heart failure in infancy. However, HCM usually improves with age.
A septal defect is a hole between two of the chambers of the heart, often referred to as having a ‘hole in the heart’. The hole can be between the upper chambers (atrial septal defects) or the lower chambers (ventricular septal defects).
Read more about congenital heart disease.
Other, less common characteristics of Noonan syndrome are briefly described below.
Some children with Noonan syndrome will have learning difficulties, which are usually mild.
To put this in context, the average intelligence quotient (IQ) score is 100. The average IQ of children with Noonan syndrome affected by a learning difficulty is around 70.
Around 50% of children with Noonan syndrome have a defect that means that their blood does not clot properly. This makes their skin more vulnerable to bruising and they may bleed excessively from cuts.
If your child is affected and needs surgery or dental work, they will need to be observed for longer than usual afterwards, in case of bleeding.
Around half of children with Noonan syndrome will have one or more eye conditions, including:
Children with Noonan syndrome have problems with their lymphatic system. Most commonly this causes a build-up of lymph fluid in their feet resulting in severe swelling. This is known as lymphoedema.
Hypotonia is decreased muscle tone. Most children with Noonan syndrome will have a degree of hypotonia, which may mean it takes them longer to reach developmental milestones during early childhood.
Children with Noonan syndrome may experience temporary bouts of hearing loss. This is caused by a build-up of fluid inside the middle ear, which is known as Otitis media.
In around 60% of boys with Noonan syndrome, either one or both of their testes fails to drop into the scrotum (the bag that holds the testicles). It is important that this is corrected through surgery at an early age, to avoid reduced fertility in later life. Many older males who have not had early corrective surgery may have a reduced sperm count.
Many babies with Noonan syndrome have feeding problems such as:
These sorts of feeding problems can cause babies to gain weight at a lower than expected rate. This is often referred to as ‘failure to thrive’. However, feeding problems usually resolve once a child reaches two years of age.
Children with Noonan syndrome may show difficult behaviour, although it is not usually severe enough to need specialist help. Common types of difficult behaviour include:
Some children with Noonan syndrome will develop problems that affect normal development of bones and joints (orthopaedic problems). For example:
Noonan syndrome is caused by a series of genetic mutations. A genetic mutation happens when there is an error in the copying process. This means some of the body’s processes will not work in the normal way.
Exactly how genetic mutations trigger the symptoms of Noonan syndrome is still unclear. However, it is thought they disrupt some of the proteins responsible for regulating cell growth and development. There is no evidence to support environmental factors as a cause, such as diet or radiation.
These mutations can be inherited (autosomal dominant inheritance) or happen entirely by chance (sporadic mutation).
There are at least eight genetic mutations linked to Noonan syndrome. The four most common are:
In an estimated 1 in 5 cases of Noonan syndrome no specific genetic mutation can be found.
Different mutations don't appear to cause different symptoms, with the following two exceptions:
Around half of all people with Noonan syndrome have a known family history of the disorder. In these cases, one of the genes responsible for the condition is passed to them from one of their parents.
In the other half of people with Noonan syndrome, the disorder is caused by a new gene mutation.
In these cases, there is no family history of Noonan syndrome but a gene changes (mutates) spontaneously for the first time. The reason why this occurs is not yet fully understood.
Noonan syndrome may be suspected if your doctor or paediatrician (doctor specialising in the treatment of children) spots some of the signs and symptoms most commonly associated with the condition.
Read more in the characteristics of Noonan syndrome.
However, in some cases, symptoms may not become apparent until the teenage years or adulthood.
In this case, you may be referred to a specialist (a clinical geneticist) for genetic testing. In most cases, Noonan syndrome can be confirmed by a blood test for the various genetic mutations. However, in about 1 in 5 cases, no specific mutation can be found, so a negative blood test will not rule out Noonan syndrome.
If Noonan syndrome has been confirmed or is strongly suspected, further tests are needed to establish the extent of the symptoms. These tests will probably include:
The echocardiogram may need to be monitored regularly to determine if there is any change in the heart function.
There is no cure for Noonan syndrome. However, it is possible to treat certain aspects of the disorder.
A full assessment of your child's heart function should be carried out as soon as Noonan syndrome has been diagnosed. This will help determine the recommended treatment for your child’s congenital heart disease.
In cases of pulmonary stenosis that are causing no or few symptoms, a policy of ‘watchful waiting’ may be recommended. This means your child will receive no immediate treatment but their heart will be carefully monitored.
In more serious cases of pulmonary stenosis a small, flexible tube, known as a catheter, can be inserted to the site of the pulmonary valve. A small balloon is passed up through the catheter and inflated to widen the affected valve. This procedure is known as a balloon angioplasty. Once the valve has been widened, the balloon is removed. Sometimes a replacement valve is required.
There are several treatments available for hypertrophic cardiomyopathy (HCM). The recommended treatment will depend on the severity of your child’s symptoms and the general state of their heart. In many cases of Noonan syndrome it will be worse in infancy but improve with age. Possible treatments include using:
As with pulmonary stenosis, watchful waiting is usually recommended for small septal defects. Many defects close by themselves as a child gets older.
In cases of mild to medium sized septal defects, it may be possible to seal the hole using a catheter. The catheter is guided to the site of the hole and then a specially designed mesh is passed through the catheter to seal it.
In cases of medium to large sized septal defects, open heart surgery will probably be required. This involves a patch being stitched directly over the hole.
Read more information about treating congenital heart disease.
Your child’s size and growth rate will be regularly assessed throughout their childhood. If your child’s growth rate is thought to be seriously reduced, a course of human growth hormone (HGH) may be suggested.
A course of HGH usually starts at around five years of age and continues until adult height is reached. A type of HGH called somatropin is used to treat children with Noonan syndrome. Somatropin is given by a daily injection using an auto-injector syringe.
Most children are able to tolerate somatropin well and side effects are uncommon, with the exception of some temporary soreness, itchiness and redness at the site of the injection.
Read more about restricted growth (short stature).
In children with Noonan syndrome, weak muscles in the mouth can sometimes cause speech and feeding problems. If your child has speech or feeding problems, they may be referred to a speech therapist for help and support.
The speech therapist will help your child develop the muscles in their mouth and show them how to use their muscles more effectively.
In particularly severe cases of poor feeding, your baby may need a feeding tube for a few months.
If you have a baby boy with an undescended testicle or testicles, corrective surgery is usually recommended before he reaches two years of age.
A surgical procedure known as an orchidopexy is the usual treatment for undescended testicles. It involves making a small cut in your child’s tummy and moving the testicle(s) into the correct position.
Read more about treating undescended testicles.
If your child is diagnosed with learning difficulties, it does not necessarily mean they cannot be taught in a mainstream school. However, children with more severe disabilities may benefit from attending a specialist school.
To ensure your child gets the support they need, it is recommended that a statement of special educational needs (SEN) is drawn up. An SEN is a type of care plan produced by both the child’s parents and their school, and is designed to meet the child’s educational requirements.
Information about treatment for other conditions associated with Noonan syndrome can be found in the list below:
Important: Our website provides useful information but is not a substitute for medical advice. You should always seek the advice of your doctor when making decisions about your health.