Hi, I was wondering if anyone else has been diagnosed with Primary congenital Ig G1 specific deficiency. My daughter and I were diagnosed with this about 18 months ago.
We have had a really hard time getting useable information in regards to this. Most information seems to cover G2, G3 and G4. Mostly, it just says G1 is very rare. I would love to hear from anyone who has been dianosed with this, or anyone that would have much information in regards to this.



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