New Way to Study the Mental Capabilities of Children Over 12 With PA or MMA
Propionic and Methylmalonic Acidemia are metabolic diseases that often come with developmental delays and disabilities in mental capabilities. About half of the children studied with PA have either delays in motor skills (like walking) or in the ability to speak. In studies of children with MMA, their tests of understanding, reasoning, and memory showed lower scores. It is important to note that, in surveys of children with PA, their responses showed that they felt generally healthy and similar to their peers.
Researchers are working on clinical studies for new treatments that may have a positive effect on mental capabilities but need to be able to prove, by some type of measurement, that there is an improvement in understanding, remembering, thinking, reasoning, and paying attention before and after the study’s treatment.
A recent study assessing different ways to measure these abilities, specifically in people with PA and MMA, found one interesting approach that seemed to be better at it.
The “Cookie Theft Picture Task”
The “Cookie Theft Picture Task” provides a specific picture to stimulate spontaneous speech about that image, which can demonstrate the ability to understand, reason, and express thoughts verbally. The test was designed for individuals ages 12 years and older.
A picture is shown of a mother washing dishes and two children, one of whom is reaching for a cookie while standing on a stool that is about to tip over. The person being tested is asked, “Tell me everything you see going on in this picture.” Their responses are recorded and then analyzed according to various measures. Most adults complete this test in 1–2 minutes. All participants ages 12 years and older were able to complete the Cookie Theft Picture Task. The analysis was able to show any weakness in the capabilities necessary to understand and respond verbally to the questions about the picture.
Until recently, little attention has been given to how people with metabolic disorders, like PA and MMA, can speak about their observations and understanding of what they experience or see. Researchers believe that this capability may be sensitive to small changes in toxic metabolite levels on a day-to-day basis and may have an important influence on day-to-day functioning.
In other words, researchers believe that changes in how children engage in conversations about their perceptions may have the potential to serve as markers that reveal subtle symptoms in PA and MMA. Studies in linguistics reveal that spontaneous speech involves motor abilities, as well as coordination, speed of thinking processes, and rapid use of working memory. These are areas that are known to be particularly affected in PA and MMA.
Source: Chapman K.A. et al. Molecular Genetics and Metabolism Reports 34 (2023) 100953
Latest from Know Rare
Discover the latest treatments for IgA Nephropathy (IgAN), a rare kidney disease. Learn how current medications and emerging therapies work to slow progression, reduce proteinuria, and protect kidney function.
Discover how patient education empowers individuals with rare diseases to better understand their diagnosis, make informed decisions, and actively participate in their treatment plans. Learn why clear, compassionate communication is key to improving outcomes in rare disease care.
A heartfelt mother’s account on five years of navigating pediatric specialist waiting rooms with her medically complex child.
A powerful personal journey through Koolen-de Vries syndrome, ADHD, and neurodivergent parenting. Discover how one mother turned diagnosis into empowerment, embracing difference, healing guilt, and raising resilient, remarkable children in a world that doesn’t always understand.
Toni Roberts lives with Epidermolysis Bullosa, a rare genetic disorder that causes the skin to be extremely fragile and prone to blistering and tearing. Toni’s condition profoundly impacted her older sister, Cady Ward. Witnessing Toni’s daily struggles and challenges, Cady was inspired to become an advocate for rare disease and take on an extraordinary challenge—run an ultra-marathon.
Dr. David Fajgenbaum was in his third year of medical school when a rare and mysterious illness derailed his plans. Crushing fatigue, abdominal pain, and multiple swollen lymph nodes progressed rapidly, and he found himself in the ICU with multiple system organ failure. Recovering from the brink of death, he was diagnosed with Castleman disease (CD), a rare condition that at the time was thought to be a lymph node disease with similarities to cancer.
Learn about Dr. Rohit Aggarwal’s efforts in creating more centers of excellence for myositis, as well as educating, empowering, and connecting patients to clinical trials.
Recognizing the need for an effective way to treat becker muscular dystrophy, researchers have been studying the cause of muscle loss, and ways to stop it from happening.
After his diagnosis of limb-girdle muscular dystrophy type 2B at age 21, Chris initially opted for a safe career path, choosing jobs with steady income, benefits, and predictability. However, this decision made him feel like something was missing. Find out how Chris was finally able to follow his heart, finding purpose and contentment in becoming a writer.
Learn more about CureGRIN, founded in 2018 by parents of children diagnosed with GRIN Disorder to help find cures and therapies for people around the world suffering from these conditions.
Learn about the incredible story of Edward Gent, a Sports Nutritionist diagnosed with MMN, who decided to create an app to help others worldwide with their disease and symptom management.
Find out about 7 research areas identified as priorities in Sickle Cell Research and about a sickle cell disease drug, which was originally approved for treatment, that has been taken off the market.
It’s no secret that it is difficult to get to a pain medicine specialist. There are just so many people in pain who cannot find relief, and are looking for help. Learn about Bliss Health, which provides access to pain management services through virtual consultations, through a dedicated team of medical professionals who specialize in the diagnosis, treatment, and ongoing management of various types of chronic and acute pain conditions.
There are over 50 million people in the United States that live with chronic pain. However, researchers studying pain have learned something important: perception of pain is personal, and may have more to do with other factors than just the physical cause of the pain.
If you are coming across high copays and struggling to afford your treatment plan, here are a few options that may help you reduce the costs of your medications.
At age 15, Becca Salky became her own medical detective, playing a key role in uncovering her diagnosis. Now, as a Clinical Research Coordinator at Massachusetts General Hospital, she focuses on spreading awareness about MOG, finding better diagnostic tools, leading clinical trials, and fighting gender disparity.
On the “Rare Insights” podcast we bridge the gap between those living with rare diseases and the biopharmaceutical industry.
Why Men’s Health Week (June 10-16) matters for the Rare Community, and how you can take part.
June is Pride Month, and at Know Rare, we are committed to celebrating the rich diversity within the rare disease community.
Journalist Lindsay Guentzel describes navigating a diagnostic odyssey and how she manages day-to-day life with myositis in an impactful webinar.
When you live with a rare disease, the joyful experiences risks can bring are all the more valuable.
This summer, NMOSD and MOGAD patients, caregivers, clinicians, nurses, researchers, and advocates are invited to join The Sumaira Foundation at Emory for TSF's Atlanta Patient Day.
Know Rare writer Gina DeMillo Wagner’s new memoir, Forces of Nature explores powerful themes related to caregiving and rare disease.
Journalist Lindsay Guentzel offers an inside look at life with the rare muscular condition.
This May, Know Rare is shining a light on myositis, a group of rare autoimmune muscle diseases that can have profound effects on daily life. This is an important time for the myositis community and the rare disease community at large: a time to share stories from those living with the condition, share more information about the current state and future of the disease, and advocate for better treatments that will ultimately enhance the quality of life for those impacted by it. Whether you're a patient, caregiver, or advocate, join us in raising awareness and supporting those affected by myositis.
Author Chris Anselmo explains why being mindful of your pace can have major benefits for your health and well-being, and offers some tips to help.