Duran family's 22q story
The Duran family shares their 22q story, and the importance of early detection and diagnosis.
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The Duran family shares their 22q story, and the importance of early detection and diagnosis.
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22q11.2 deletion syndrome, also known as DiGeorge, is caused by a missing section of chromosome 22. It is more common than other conditions routinely screened for prenatally such as cystic fibrosis, s
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Until recently, there has not been a reason to diverge from the standard approach of giving Rh immune globulin to all Rh negative patients. That has changed with the introduction of fetal RhD NIPT, no
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