Experts say rare disorder only affects 1 or 2 people in a million, and is often not recognized
A rare neurological disorder that affects about one or two people per million is in the spotlight in the wake of an emotional social media post by pop star Céline Dion, who described her challenges with stiff-person syndrome
Dion, 54, says she’s been forced to cancel shows after years of struggling with muscle spasms and other health problems related to the debilitating neurological condition
Because of its rarity, very few experts can speak knowledgeably on the disorder
John Hopkins Medicine, a facility in Baltimore, Md., has a Stiff Person Treatment Center (new window). In a video explainer on the facility’s website, Dr. Scott Newsome, a neurologist at Johns Hopkins Medicine, says the syndrome is a very rare but devastating
autoimmune disease. There’s no clear cause, and the disorder is still being researched
How does it affect people?
In the video, Newsome says the progressive condition shows up initially as a painful rigidity in muscles, causing spasms and imbalance. Newsome says the syndrome often causes a rigidity in the torso, lower back, abdominal and leg areas, affecting gait and balance
Just walking down the street, they could have a spasm and fall,
Newsome explains
Sufferers are sensitive — anxiety and even loud noises can lead to an excruciating spasm, according to Dr. Marinos Dalakas, professor of neurology and director of the neuromuscular division at Thomas Jefferson University School of Medicine in Philadelphia
He says sufferers may walk like the tin man
in The Wizard of Oz as their muscles spasm and contract
It is not pleasant. They walk like a statue,
Dalakas told CBC in an interview
He lauds Dion for speaking out about her personal struggle with the syndrome
It’s very important because the syndrome will become more known … and so the more people understand, the more physicians know about the syndrome, the earlier the diagnosis is made, the better treatment and more treatment will happen,
said Dalakas
In a post (new window) on the National Library of Medicine website, Texas neurologist Alexandra Muranova says the condition has an insidious onset with gradual worsening over time and, if left untreated, can lead to permanent disability and mortality
Newsome said that on average, it can take about seven years to reach a diagnosis. He says there is some evidence that the syndrome is related to an imbalance of gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter in the central nervous system
GABA regulates the nervous system, so if its levels are low, he says that can create spasticity
or hyper-excitability in the nervous system that looks like spasms, rigidness and tightness that leads to the disability
Sufferers often not believed
Newsome stresses that the disorder is not fully understood, but is believed to have a relationship to T-cells — a part of the immune system that attacks foreign particles
We are still learning,
said Newsome, who studies patients at his clinic to improve treatment
He said that stiff-person syndrome affects predominantly older women. It was first described in the 1950s as stiff-man syndrome, despite the fact that the first case affected a female
Because it can take years to diagnose — as some hallmark traits do not immediately appear — Newsome warned that many sufferers are not initially believed
Treatments
Sufferers are treated by specialists with an expertise in the brain and muscles, along with various experimental drugs
According to the National Institute of Neurological Disorders and Stroke (NINDS), patients have responded to high doses of diazepam or anti-convulsants, gabapentin and tiagabine. Some researchers have tried immunoglobulin treatment in reducing stiffness and lowering sensitivity to noise, touch and stress
NINDS researches (new window) the syndrome in its laboratories at the National Institutes of Health (NIH), and says current research is focused on understanding the cause of the disease and the role of certain antibodies
CBC News
