It is very hard to talk about and explore, much less cure, a syndrome if you don’t define it first. While 22q13 deletion syndrome seems like it should be straightforward — a deletion of 22q13 — life is rarely that simple. In 2012 I was offered a chance to bring people together to address the question of how to define Phelan McDermid syndrome (PMS). I took the role and opportunity seriously. I decided to make a slide presentation that would set the stage for parents, scientists and clinicians to discuss a definition for the syndrome. As it turned out, the offer was rescinded. Without any modification, I present the final slide from my talk, 4.5 years later. In my opinion, the discussion is overdue.
The color coding is important. Things in green are PMS. Things in rust red are not PMS. Dashed lines are just to make it easier to see. The scheme covers nearly every circumstance, including pathology of regulatory sites. The only unaddressed issue is what might be considered phenotypic. It seems to me now that any intellectual disability that is not syndromic in some other way (e.g., metachromatic leukodystrophy caused by the deficiency of arylsulfatase A, OMIM #250100), should be considered the core phenotypic trait of PMS. Regardless, the slide represents the only detailed framework I have ever seen for a definition of PMS.
There is a great interest in SHANK3 and its relationship with 22q13 deletion syndrome. Using the scheme, above, and other information that we know about SHANK3 and 22q13 chromosomal deletions, I recently put together this chart:
In this case, the dashed line indicates that autism spectrum disorder may accompany intellectual disability and still be part of PMS. The chart shows that many SHANK3 mutations are not PMS. They are either nothing (have no phenotype) or some other neuropsychiatric disorder. When 22q13 deletions include SHANK3 (even just a part of SHANK3), they can be PMS. In fact, they are rarely not PMS. Some SHANK3 mutations lead to the phenotypic traits of PMS. Mutations of SHANK3 that confer a different primary phenotype (e.g., schizophrenia or autism spectrum) should not be lumped into the PMS category.
There are other ways to define a disorder, but the worse thing we can do is not define it at all.
Why don’t we have better drugs for 22q13 deletion syndrome?
What do parents want to know?
Is 22q13 deletion syndrome a mitochondrial disorder?
Educating children with 22q13 deletion syndrome
How to fix SHANK3
Have you ever met a child like mine?
How do I know which genes are missing?
How can the same deletion have such different consequences?
22q13 and the hope of precision medicine
22q13 Deletion Syndrome: hypotonia
Understanding gene size
Gene deletions versus mutations: sometimes missing a gene is better.
Is 22q13 deletion syndrome a ciliopathy?
Understanding translocations in 22q13 deletion syndrome: genetics and evolution
Understanding deletion size
Can 22q13 deletion syndrome cause ulcerative colitis?
Can 22q13 deletion syndrome cause cancer?
22q13 deletion syndrome – an introduction
4 thoughts on “Defining Phelan McDermid syndrome”
metachromatic leukodystrophy now I’m confused on that. They recently tested my son’s blood and even did am MRI.
Not to worry! There are a number of well known mutation syndromes caused by genes of 22q13. Metachromatic leukodystrophy is a disease associated with mutations of the ARSA gene. ARSA is the gene right next to SHANK3. That is just one example. There is also a syndrome associated with mutation of ATXN10 and other 22q13 genes. The point I make in the blog is simple. If you have one of these other syndromes, a doctor would not diagnose it as PMS. That is why not all SHANK3 mutations are PMS.
Trying to find the blog that discussed that people with this profile do not create new neurons in the memory center of the brain! Can you point me towards that blog, my apologies for this request!
Producing new neurons is usually called neurogenesis. During development, neurogenesis is a very active process. It crucial for any brain, but especially the human brain with so many neurons. There is also a process called adult neurogenesis. It seems important for new learning, especially in the hippocampus. The hippocampus is in some ways a memory center.
One blog that discusses neurogenesis in the cortex during development is the blog on PHF21B. https://arm22q13.wordpress.com/2021/12/11/pms-gene-phf21b-is-critical-for-normal-brain-development/
Another blog discusses brain recovery from injury. It discusses the neuroprotective role of CELSR1. There is evidence that CELSR1 is involved in adult neurogenesis. I mention it here
And, the scientific paper is here:
I hope this is what you are looking for.