22q In the News
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As part of its mission to promote awareness regarding 22q11.2 deletion syndrome, The 22q Family Foundation strives to provide timely content from credible sources through channels that include but are not limited to this website. All content is made available for information purposes only. The Foundation gives no assurance or warranty, nor makes any endorsement or other representation, as to the accuracy, completeness, or validity of such content. Each person accessing this site is responsible for making his/her own assessment of the information provided.
Conclusion: These patients widen the spectrum of clinical signs of the 22q11
Mia Brueggeman is what her family deems “a miracle baby,” shining light into their lives each and every day and with everyone she meets in her battle with DiGeorge Syndrome.
WHEN Michelle and Mark Murphy lost their baby boy Billy after he was born with Digeorge Syndrome, they set up a fund in his memory for Crumlin hospital.
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