Could it be a sign of the rare disease known as Hunter syndrome?
Sleep apnoea in children
Sleep apnoea (temporarily stopping breathing during sleep) is relatively common in children; it affects around 1–4% of children. There are a number of causes of sleep apnoea, mainly related to physical obstruction of the airway (by the tongue or due to an unusual shape of the mouth or throat).
One possible cause for sleep apnoea in children is Hunter syndrome, which is also known as mucopolysaccharidosis type II (MPS II).
- Hunter syndrome is a rare, genetic condition that affects many systems of the body.
- It is estimated to affect around one in every 162,000 children born, and because of its genetic mechanism, the majority of the children affected are boys.
- Hunter syndrome is a progressive disease, and some symptoms can reach a point at which they become irreversible. Early diagnosis is important to ensure appropriate management can begin as soon as possible.
Sleep apnoea is relatively common, but if your child is also experiencing unusual clusters of common childhood complaints, such as hernias and frequent ear infections, Hunter syndrome should be considered.
If you think that your child may be showing two or more of the symptoms of Hunter syndrome, speak to your doctor.
Other signs and symptoms that may indicate Hunter syndrome include:
- Particular facial features, such as a prominent brow, broad nose and thick lips
- Hernias (umbilical or inguinal)
- Large head
- Joint stiffness, which may lead to restricted movement
- Frequent or long-term diarrhoea
- Delays in childhood development (e.g. delayed walking, delayed speech)
It is important to remember that many of these signs and symptoms are common in childhood, and it is the combination of them that may indicate Hunter syndrome