This rare metabolic disorder can affect the lungs, heart, joints, connective tissue, brain and nervous system. Treatments may help complications.
Hunter syndrome is a very rare, inherited genetic disorder caused by a missing or malfunctioning enzyme. In Hunter syndrome, the body doesn't have enough of the enzyme iduronate 2-sulfatase. This enzyme's job is to break down certain complex molecules, and without enough of this enzyme, the molecules build up in harmful amounts.
The buildup of massive amounts of these harmful substances eventually causes permanent, progressive damage affecting appearance, mental development, organ function and physical abilities.
Hunter syndrome is far more common in boys. The condition is one type of a group of inherited metabolic disorders called mucopolysaccharidoses (MPSs). Hunter syndrome is also known as MPS II.
There's no cure for Hunter syndrome. Treatment involves managing symptoms and complications.
Hunter syndrome symptoms vary and range from mild to severe. Symptoms aren't present at birth, but often begin around ages 2 to 4 as the harmful molecules build up.
Signs and symptoms may include:
Hunter syndrome is very uncommon, but if you notice changes in your child's facial appearance, a loss of previously acquired skills, or other signs or symptoms listed above, talk to your child's primary care doctor. He or she can help you decide if you need to see a specialist or seek further testing.
Hunter syndrome develops when a defective chromosome is inherited from the child's mother.
Because of that defective chromosome, an enzyme that's needed to break down complex sugar molecules is missing or malfunctioning. Without this enzyme, massive amounts of these complex sugar molecules collect in the cells, blood and connective tissues, causing permanent and progressive damage.
There are two major risk factors for developing Hunter syndrome:
A variety of complications can occur with Hunter syndrome depending on the type and severity of the disease. Complications can affect the lungs, heart, joints, connective tissue, and brain and nervous system.
An enlarged tongue, thickened gums, and thickening of the nasal passages and windpipe (trachea) make breathing difficult. Children often have chronic ear and sinus infections, respiratory infections, and pneumonia.
Sleep apnea, a condition in which breathing is intermittently interrupted during sleep, is often present because of airway constriction.
Thickening of heart tissue can cause improper closing of heart valves. As a result, the heart and other parts of the body don't receive blood efficiently. As the disease progresses, these conditions often become worse and typically result in heart failure.
The thickening of tissue can also cause narrowing of the aorta and other blood vessels. This in turn can result in high blood pressure and narrowing of arteries in the lungs.
The storage of undigested complex sugar molecules in connective tissues results in abnormalities in bones, joints and ligaments. This reduces your child's growth, causing pain and physical malformations and making it difficult for him or her to move.
Joint stiffness is caused by swelling of joint connective tissues and abnormalities of cartilage and bones. If your child is in pain, he or she will likely move less, which can lead to more stiffness and pain.
The group of abnormalities typically seen in the bones of people with Hunter syndrome is called dysostosis multiplex. Children with these abnormalities can develop irregularly shaped vertebrae and spines, ribs, arms, fingers, legs, and pelvises.
Bone abnormalities may cause many people with Hunter syndrome to be abnormally short. Those with milder cases may reach normal or near-normal height.
Hernias are common in Hunter syndrome. A hernia occurs when soft tissue, usually part of the intestine, pokes through a weak spot or tear in the lower abdominal wall.
Hernias associated with Hunter syndrome can become quite large and are often one of the first signs of the disorder. Enlargement of the liver and spleen may increase pressure in the abdomen, causing a hernia.
A variety of neurological complications may be present and continue to develop in children with Hunter syndrome.
Many neurological problems are caused by buildup of excess fluids in your child's brain. Pressure from these fluids can cause other problems that may cause severe headaches, interfere with vision and change your child's mental state.
Your child may also develop a condition in which the membranes that surround the spinal cord may become thick and scarred. This causes pressure and compression of the upper spinal cord. As a result, your child may develop fatigue in his or her legs and gradually weaken and become less physically active.
Other disorders, such as carpal tunnel syndrome, can result from nerve compression that happens because of bone deformities and storage of complex sugar molecules in tissues.
Abnormal behavior can develop in children with more-severe cases of Hunter syndrome. Often your child's mental development will become affected between the ages of 2 and 6.
Some children are hyperactive and have trouble paying attention or following directions. Your child may also behave aggressively and seem unable to sense danger. As your child's overall physical functioning declines, these behavior problems tend to become less severe.
Seizures also may occur in children with Hunter syndrome.
Recovery times from normal childhood illnesses may be longer for children with Hunter syndrome. As a result, be sure to take general preventive measures — for example, get your child a flu shot and ensure your child receives all necessary vaccinations.
Hunter syndrome is a genetic disorder. Talk to your doctor or a genetic counselor if you're thinking about having children and you or any members of your family have a genetic disorder or a family history of genetic disorders.
If you think you might be a carrier, genetic tests are available. If you already have a child with Hunter syndrome, you may wish to seek the advice of a doctor or genetic counselor before you have more children.
Babies born with Hunter syndrome almost always appear healthy at birth. Changes in facial features are often the first noticeable sign that something's not right. Hunter syndrome progresses slowly and its signs and symptoms overlap with a number of other disorders, so a definitive diagnosis may take awhile.
A urine sample can be checked for the deficient enzyme or for excess amounts of the complex sugar molecules associated with this disorder. A genetic analysis can confirm the diagnosis.
Prenatal testing of the fluid that surrounds the baby (amniocentesis) or of a tissue sample from the placenta (chorionic villus sampling) can verify if your unborn child carries a copy of the defective gene or is affected with the disorder.
Prenatal testing of the fluid that surrounds the baby or of a tissue sample from the placenta can verify if your unborn child carries a copy of the defective gene or is affected with the disorder.
Removal of tonsils and adenoids can open up your child's airway and help relieve sleep apnea. But as the disease progresses, tissues continue to thicken and these problems can come back.
Breathing devices that use air pressure to keep the airway open — such as continuous positive airway pressure (CPAP) or bilevel positive airway pressure (BiPAP) devices — can help with upper airway obstructions and sleep apnea. Keeping your child's airway open can also help avoid low blood oxygen levels.
Your child's doctor will want to watch closely for cardiovascular complications, such as high blood pressure, a heart murmur and leaky heart valves. If your child has severe cardiovascular problems, your doctor may recommend surgery to replace heart valves.
Because most children with Hunter syndrome don't heal well and often have complications after surgery, options are limited for addressing skeletal and connective tissue complications. For example, surgery to stabilize the spine using internal hardware is difficult when bones are fragile.
Your child's joint flexibility can be improved with physical therapy, which helps address stiffness and maintain function. But physical therapy can't stop the progressive decline of joint motion. Your child may eventually need to use a wheelchair because of pain and limited stamina.
Surgery can repair hernias, but because of weakness in connective tissues, results usually aren't ideal. The procedure often needs to be repeated. One option is to manage your child's hernias with supportive trusses rather than surgery because of the risks of anesthesia and surgery.
Problems associated with the buildup of fluid and tissue around the brain and spinal cord are difficult to address because of the inherent risks in treating these parts of the body.
Your child's doctor may recommend surgery to drain excess fluids or remove built-up tissue. If your child has seizures, your doctor may prescribe anticonvulsant medications.
If your child develops abnormal behavior as a result of Hunter syndrome, providing a safe home environment is one of the most important ways you can manage this challenge. Treating behavior problems with medications has had limited success because most medications have side effects that can worsen other complications of the disease, such as respiratory problems.
The sleep patterns of a child with Hunter syndrome can become more and more disorganized. Medications including sedatives and especially melatonin can improve sleep.
Keeping a strict bedtime schedule and making sure your child sleeps in a well-darkened room also can help. In addition, creating a safe environment in your child's bedroom — putting the mattress on the floor, padding the walls, removing all hard furniture, placing only soft, safe toys in the room — may help you rest easier.
Some treatments have shown potential for slowing the disease's progress and lessening its severity, but long-term effects are unknown.
Enzyme therapy. This Food and Drug Administration-approved treatment uses man-made or genetically engineered enzymes to replace your child's missing or defective enzymes and ease the disease symptoms. This treatment is given once a week through an intravenous (IV) line.
Given early enough, enzyme replacement therapy may delay or prevent some of the symptoms of Hunter syndrome. It's unclear, however, if the improvements seen with this therapy are significant enough to raise quality of life for people with the disease. In addition, benefits in thinking and intelligence haven't been seen with enzyme replacement therapy.
Serious allergic reactions can occur during enzyme replacement therapy. Other possible side effects include a headache, fever and skin reactions. Side effects may lessen over time or with a dose adjustment, however.
Joining a support group for parents of children with Hunter syndrome can be a great way to obtain practical information, daily living strategies and encouragement from other parents in similar situations to your own. Ask your doctor if there's a group in your area.
The intense supervision that may be needed for your child can cause you and other caregivers to become physically, mentally and emotionally exhausted. If respite care is available, take advantage of it so that you can have a break and be more effective in the long run to meet the day-to-day challenges of caring for your child.
Check with your county and state for resources that may be available to you as a parent of a child with special needs.
Due to a narrow airway, people with Hunter syndrome often have difficulty receiving a breathing tube during general anesthesia. You may wish to note this on child care or school forms so that emergency personnel can be alerted to this fact, in case your child has an emergency and you're not there. An experienced anesthesia specialist should perform the intubation of a person with Hunter syndrome.
You'll probably first bring up your concerns about your child with his or her primary care doctor. Your child's doctor then will likely direct you to specialists for a definitive diagnosis and treatment. However, your child's primary care doctor generally still stays involved to help coordinate your child's health care needs.
Some of the specialists who may be involved in your child's care include an ear, nose and throat specialist (otolaryngologist), a heart specialist (cardiologist), a brain and nerve specialist (neurologist), an eye specialist (ophthalmologist), a dietitian, and physical, occupational and speech therapists. A geneticist may be involved in making the diagnosis and in counseling about future pregnancies.
Here's some information to help you get ready for your appointment, and what you might expect from your child's doctor.
Preparing a list of questions will help you make sure you cover all of the points that are important to you. Some basic questions you might want to ask your doctor include:
In addition to the questions that you've prepared to ask your doctor, don't hesitate to ask additional questions that occur to you during your appointment. If it helps, take notes.
At the end of your appointment, you may wish to summarize the information you've received with your doctor to make sure you understand it. Ask for a copy of your doctor's clinical note for future reference and communication with other facilities.
Your doctor is likely to ask you a number of questions. Being ready to answer them may reserve time to go over any points you want to spend more time on. Your doctor may ask:
May 4th, 2021