MKRN3 Mutation (chromosome 15q11.2)
This was back when they still in the early days of discovering CPP causes and the ways it can manifest.
I gave birth to a child with neonatal CPP and after an odysee of doctors and an extensive bunch of tests it was diagnosed with a special treat for me. I gave the Mutation - that was already, but mildly, active in me - full blown outcoming to my daughter in utero.
Like i said, it was a rare anomaly.
Back then i was completly overwhelmed and not thinking further than what my child needs and how we can provide that. And of course how to navigate the years to come.
But now, my kids are grown and because they think about families of their own, this topic made it back into my mind.
I researched it again and looked up the possible implications for future gens and what sience and medicine figured out since then.
Now here is my question or maybe a thought:
Should i get registered and give my weird genomes into a programm/project for future studies?
Does it still makes sense to do so?
Is this still something science needs?