F508del and R117H in our newborn


New member
I recently read an article though in which they actually think this combo of mutations is quite common but always went undiagnosed before newborn screening due to lack of symptoms, therefore, they think a lot of adults are living normal healthy lives with our babies exact mutations. This was reassuring to me. Anyways, I just wanted to say hi as it's nice to find others in the same boat who can understand. I would love to keep communication open with you ladies.

pikashow apk
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