What do you think one should do if a fetus has been diagnosed with Acalvaria? Are the consequences of Acalvaria on the brain development of the fetus documented and can we hear more about this? What kind of life is a person with Acalvaria able to have after birth - what medical care will they need, and what are the consequences?
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Hi, I was wondering what your experience is with Acalvaria? I'm trying to connect with anyone with experience or knowledge on Acalcaria. I look forward to hearing from you soon. Thank you.
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