#CSNK2A1
The phenotype holds up in rat neurons, a CSNK2A1-K198R mouse model, & patient iPSC-derived neurons. Same mechanism, three systems.
August 18, 2026 at 2:21 PM
Please consider a donation for #GivingTuesday to the CSNK2A1 Foundation, whose mission is to support, research, find treatments and answers for those living with Okur-Chung Neurodevelopmental Syndrome, like my child. Thank you for your support! 💙💚 loom.ly/Z26kYM4
Unite with Us to Change Lives
Transform Lives Today! Join Us This Giving Tuesday to Bring Hope to Families with OCNDS This Giving Tuesday, we invite you to make a difference for children and families affected by Okur-Chung Neuro...
loom.ly
December 3, 2024 at 7:32 PM
Tomorrow, Sunday 5 April, the Cathedral Tower will be lit green/blue for Okur-Chung Neurodevelopmental Syndrome. Find out more at csnk2a1foundation.org

#ocnds #csnk2a1 #moveintoaction #timeisnow #BoundlessPossibilities #OCNDSAwareness
April 4, 2026 at 5:50 PM
Patient advocacy groups deliver their top three unmet needs and main asks of industry to best serve their rare community. This week’s insights come from Jennifer Sills, president and founder, The CSNK2A1 Foundation

https://ow.ly/tKQ350ZyYIz
August 17, 2026 at 11:00 AM
OCNDS is rare, but with your help, we can make an outsized impact. Research and support for families navigating this journey are critically underfunded. That’s why I’m asking my network to join me in supporting CSNK2A1 Foundation
December 3, 2024 at 8:26 AM
🌎 Today is International OCNDS Awareness Day 🌎

🔹 Join us in spreading the word!
🔹 Support research to drive progress.
🔹 Celebrate the amazing OCNDS community.

💙 Together, we can shine a light on OCNDS and create a future filled with hope. 💙

#OCNDSAwareness #CSNK2A1
April 5, 2025 at 3:50 PM
Today is Giving Tuesday—a day to reflect on the power of generosity and its ability to transform lives.

For me, this day holds special significance. As the parent of a beautiful girl with OCNDS (Okur-Chung Neurodevelopmental Syndrome), a rare condition caused by a mutation in the CSNK2A1 gene.
December 3, 2024 at 8:26 AM
Creatine kinase levels in serum (marker for muscle damage) were normal and MRI of the muscle showed no abnormalities. With improved genetic diagnostic tools authors then discovered a pathogenic variant in CSNK2A1, which fit with the symptoms of the patient.
February 19, 2026 at 10:05 AM
A great end to a beautiful day in Edmonton! ~25 friends gathered last night for OCNDS Awareness Day by the High Level Bridge, lit blue and green for OCNDS & the CSNK2A1 Foundation.

#OCNDSAwareness
#CSNK2A1Foundation #AwarenessDay
#OCNDS
#BoundlessPossibilities #yeg
#HighLeveBridge
#Edmonton
April 7, 2025 at 1:49 PM
CSNK2A1 & CSNK2B Foundations Launch CK2 Butterfly Collective, Uniting Sister-Gene Communities
rcnamericaca.blogspot.com/2025/12/csnk...
CSNK2A1 & CSNK2B Foundations Launch CK2 Butterfly Collective, Uniting Sister-Gene Communities
rcnamericaca.blogspot.com
December 1, 2025 at 10:49 PM
Measles outbreak means my immunocompromised son can't leave the house without extreme safety measures
My teenage son has Okur-Chung neurodevelopmental syndrome (OCNDS), an ultra-rare genetic disorder caused by a mutation on the CSNK2A1 gene, which creates the CK2 protein present in every cell in the body. Each patient is affected differently, but common symptoms include autism, intellectual disabilities, short stature, low muscle tone, and speech delay. Last year, he developed autoimmune encephalitis, which resulted in a two-month hospitalization. He is currently undergoing treatment that includes regular intravenous immunoglobulin infusions and a transplant rejection medication that severely suppresses the immune system. Ever since the Covid pandemic began, my family has completely changed our lives to protect his health. I work remotely, foregoing work travel and in-person meetings to limit the chance of catching Covid or any other virus. My husband left the workforce to become a stay-at-home parent and homeschool our son to limit his exposure to illness. When we venture out to places like the local library, museum, or farm near our house, we stay safe by masking and social distancing. Advertisement Those precautions are now particularly urgent. North Carolina is one of the 32 states currently facing a measles outbreak. The disease is primarily spreading through school-age children and popping up in some...
www.statnews.com
April 21, 2026 at 7:23 AM
Opinion: Measles outbreak means my immunocompromised son can't leave the house without extreme safety measures
My teenage son has Okur-Chung neurodevelopmental syndrome (OCNDS), an ultra-rare genetic disorder caused by a mutation on the CSNK2A1 gene, which creates the CK2 protein present in every cell in the body. Each patient is affected differently, but common symptoms include autism, intellectual disabilities, short stature, low muscle tone, and speech delay. Last year, he developed autoimmune encephalitis, which resulted in a two-month hospitalization. He is currently undergoing treatment that includes regular intravenous immunoglobulin infusions and a transplant rejection medication that severely suppresses the immune system. Ever since the Covid pandemic began, my family has completely changed our lives to protect his health. I work remotely, foregoing work travel and in-person meetings to limit the chance of catching Covid or any other virus. My husband left the workforce to become a stay-at-home parent and homeschool our son to limit his exposure to illness. When we venture out to places like the local library, museum, or farm near our house, we stay safe by masking and social distancing. Advertisement Those precautions are now particularly urgent. North Carolina is one of the 32 states currently facing a measles outbreak. The disease is primarily spreading through school-age children and popping up in some...
www.statnews.com
April 21, 2026 at 6:01 AM
Penelope is using Citizen Health's AI Advocate to generate IEP goals, summarize a hospital stay for a new PCP, and pull lists of past medications they’ve tried. It makes caring for her son with #OCNDS easier.

“You’ve Got to Check It Out!”

#CSNK2A1 #TheGreatUnlock #RareDisease #AccelerateCures
October 31, 2025 at 9:58 PM
📃Scientific paper: CircNDST1 promotes papillary thyroid cancer progression via its interaction with CSNK2A1 to activate...

➡️ Continued on ES/IODE

August 14, 2024 at 1:17 AM
📃Scientific paper: CircNDST1 promotes papillary thyroid cancer progression via its interaction with CSNK2A1 to activate...

➡️ Continued on ES/IODE

April 22, 2024 at 10:17 AM
Characterizing CSNK2A1 Mutant-Induced Morphological Phenotypes in Zebrafish (Danio rerio): Insights into Okur-Chung Neurodevelopmental Syndrome (OCNDS) https://www.biorxiv.org/content/10.1101/2024.01.09.574075v1
Characterizing CSNK2A1 Mutant-Induced Morphological Phenotypes in Zebrafish (Danio rerio): Insights into Okur-Chung Neurodevelopmental Syndrome (OCNDS) https://www.biorxiv.org/content/10.1101/2024.01.09.574075v1
Okur-Chung Neurodevelopmental Syndrome (OCNDS) is a rare autosomal dominant disorder caused by mutat
www.biorxiv.org
January 11, 2024 at 11:16 PM
Characterizing CSNK2A1 Mutant-Induced Morphological Phenotypes in Zebrafish (Danio rerio): Insights into Okur-Chung Neurodevelopmental Syndrome (OCNDS) https://www.biorxiv.org/content/10.1101/2024.01.09.574075v1
Characterizing CSNK2A1 Mutant-Induced Morphological Phenotypes in Zebrafish (Danio rerio): Insights into Okur-Chung Neurodevelopmental Syndrome (OCNDS) https://www.biorxiv.org/content/10.1101/2024.01.09.574075v1
Okur-Chung Neurodevelopmental Syndrome (OCNDS) is a rare autosomal dominant disorder caused by mutat
www.biorxiv.org
January 11, 2024 at 11:16 PM
CSNK2A1 confers gemcitabine resistance to pancreatic ductal adenocarcinoma via inducing autophagy #PancreaticCancer 🧪 www.sciencedirect.com/science/arti...
CSNK2A1 confers gemcitabine resistance to pancreatic ductal adenocarcinoma via inducing autophagy
www.sciencedirect.com
July 8, 2025 at 10:46 AM