22q11.2 Deletion Syndrome Overview
22q11.2 Deletion Syndrome Overview
Sep 24, 2018
checkrare.com
We’ve known from day one that Angelica has 16p11.2 duplication — a rare genetic condition that can affect growth, feeding, speech, development, and more. Even with a diagnosis, we’ve realized how much is still unknown. We’ve felt a bit stuck locally — not because anyone’s at fault, but because there just isn’t a lot of knowledge around it. After talking with our genetics team at CHOP for the little peanut, we were connected to a doctor at Boston Children’s Hospital who specializes in this duplic
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We’ve known from day one that Angelica has 16p11.2 duplication …
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