We will continue to share the importance of this unseen threat.

Delayed diagnosis of hyperammonemia can lead to neurological damage or death.

CHECK AMMONIA

#checkammonia #neurologicaldamage #hyperammonemia #nucdf #metabolicdisorders #geneticdisorders #ureacycledisorders #UCDs

Did you know?

There are 6,000+ identified rare diseases.

Help us celebrate #rarediseaseday and raise awareness for the 300 million people worldwide living with a rare disease, their families and carers.

#RareDiseaseDay #NUCDF #UCDs #metabolicdisorders #ureacycledisorders

We’re revamping our membership opportunities! Now is your chance to be an official member of the National Urea Cycle Disorders Foundation.

You can join us and help our mission.

Find more information – and join – here: nucdf.org/donate/annua...

#nucdf #ureacycledisorders #rarediseases

Amy Magyar's son Mitchell was born with a urea cycle disorder. She sat down for an interview as a part of our caregiver support initiative. Here she shares her family's story: www.youtube.com/watch?v=HxmD...

#caregiver #caregiversupport #caregiverlife #ureacycle #ureacycledisorders

A cohort study using CHNC data characterizes the NICU course and outcomes for infants with neonatal-onset urea cycle disorders. Review the study and results!➡️ buff.ly/hw87ve9

#NICUResearch #UreaCycleDisorders #Neonatology

🌏 From Kyoto to Seattle: PNRI’s Dr. Aimée Dudley joined international experts at the 6th International Symposium on #UreaCycleDisorders. We’re proud to partner with @nucdf.bsky.social and The Citrin Foundation – working together to move UCD research and treatment forward. 💙
#rarediseaseawareness

Happy holidays from our families to yours!

#UreaCycleDisorders #RareDisease #UCDs