About Rett Syndrome
Imagine the symptoms of Autism, Cerebral Palsy, Parkinson’s, Epilepsy and Anxiety Disorder…all in one little child.
Rett Syndrome is a serious lifelong neurological disorder that is caused by random mutations in a gene called MECP2. Diagnosed primarily in girls, symptoms typically appear in toddlerhood. Many children with Rett are unable to speak, walk or use their hands. Breathing problems, feeding tubes, seizures, anxiety, gastrointestinal and orthopedic issues are common.
Despite the debilitating nature of the disorder our children are so much more than a laundry list of symptoms. Their beauty and their strength inspire and motivate us.
Rett Syndrome stands apart from other neurological disorders due to the dramatic reversibility of symptoms in animal models. Our confidence that Rett Syndrome is curable guides our every decision.
Although rare, boys can also have Rett Syndrome. There are several specific genetic scenarios that can happen. Please visit our Genetics Primer to learn more. With the exception of the MECP2 Reactivation strategy all the research that RSRT supports is also applicable to boys.
What is Rett?
Rett Syndrome is a severe neurological disorder that begins to manifest itself during the toddler years. After a seemingly normal first year the child begins to lose previously acquired skills. This regression can happen quickly over a number of days or very gradually over months. Often the first noticeable symptoms include low muscle tone (hypotonia), eye crossing, decreased interactions with people and surroundings and loss of hand function. The hallmark symptom of Rett is repetitive hand movements that can be constant especially in the younger children.
As time passes additional symptoms may include loss of speech, trouble with balance and motor coordination, irritability and crying, disrupted sleep patterns. Many children develop seizures, anxiety, breathing problems, gastrointestinal and orthopedic issues as well as oral motor difficulties.
It is important to note that Rett is a spectrum disorder with children exhibiting a broad range of severity. Some children have some language, can run and feed themselves while others are unable to independently sit up. The symptoms in Rett are, unfortunately, many and often times debilitating. Our children however are so much more than their symptoms. They are beautiful, they are powerful, they are resilient. They move us to move mountains on their behalf.
What Causes Rett?
Rett is caused by errors in a gene called MECP2 which is located on the X chromosome. All of us have an MECP2 gene in every one of our cells that makes a protein also called MECP2. Children with Rett have a mutation in the gene that causes the protein to not work properly. The MECP2 protein is present throughout the body but it is especially important in the brain where it helps keep brain cells functioning properly.
To better understand your child’s mutation and what it means for her future please visit our Genetics Primer.
Why Mostly Girls?
Many studies have provided evidence that the vast majority of MECP2 mutations originate in the sperm. Since fathers give an X to their daughters and a Y chromosome to their sons the MECP2 mutation in a sperm can only be transmitted from father to daughter. This is the reason why Rett is seen primarily in girls.
When boys have Rett their MECP2 mutation comes from their mother’s egg. Sometimes however the Mutation can also originate in a single cell as the male embryo is developing. This is called somatic mosaicism.
Scientific papers over the years have hypothesized that because male fetuses only have one X their disease would be so severe that they might not develop to full term and the mothers might miscarry. However, there is no clinical data to support this hypothesis.
Due to the sheer volume of sperm that is continuously made it is likely that all men produce sperm with MECP2 mutations. One in about 20,000 eggs will be fertilized with a sperm that has an MECP2 mutation in it — the cruel reality of genetic roulette.
It is estimated that one in ten thousand girls will be born with Rett Syndrome. This means about 15,000 girls and women in the US and 350,000 worldwide have the disorder.
Rett Syndrome is classified as a “rare disease” (by definition, less than 200,000 affected individuals in the US) by the Office of Rare Diseases of the National Institutes of Health. This designation qualifies the condition for orphan drug status from the FDA which comes with certain perks for pharmaceutical companies like tax deductions and marketing exclusivity on a drug for an extended time period.
Rett Syndrome is a clinical diagnosis given by a physician based on the child’s history and symptoms. An MECP2 mutation is not required to have a clinical diagnosis of Rett Syndrome. In other words, it is possible to have a diagnosis of Rett without genetic confirmation or the other way around, an MECP2 mutation without a clinical diagnosis of Rett Syndrome.
If your child’s symptoms are consistent with Rett Syndrome but your child has tested negative for an MECP2 mutation please ensure that testing included sequencing all four exons of MECP2 and that deletion testing was done as well (sometimes called MLPA). If you have questions about your child’s testing result please contact us.
Symptoms and Health Problems
An individual with Rett will have a variety of problems that may include movement issues (apraxia, rigidity, dyskinesia, dystonia, tremors), seizures, gastrointestinal problems (reflux, constipation), orthopedic issues (contractures, scoliosis, hip problems), autonomic issues (breathing irregularities, cardiac problems, swallowing) as well as sleep problems and anxiety.
Having compassionate doctors in place that will listen to you is key. Besides a pediatrician you may need a neurologist, a gastroenterologist and an orthopedist. It’s important to note that not every child will have every symptom so the team of doctors required may vary.
Since most primary care doctors have limited experience with Rett Syndrome a consensus on guidelines about how to care for individuals with Rett Syndrome was recently published. We hope this publication will be helpful to you and we can encourage you to share it with your child’s doctors.
There are no treatments yet specific to Rett Syndrome. Medications used to treat seizures, anxiety, reflux, constipation, sleep problems, movement issues and more are often used in Rett as well. Surgeries to insert feeding tubes or correct scoliosis or other orthopedic problems are not unusual.