We hypothesized that most patients with the syndrome and a history of hypocalcemia have inadequate parathyroid function, which would be manifested by intact parathyroid hormone (PTH) levels below ...

A recent study led by UC Davis Health researchers provides new insights into the molecular changes linked to the rare genetic condition 22q11.2 deletion syndrome, or 22q. It found unique ...

The second-most common genetic disorder in children is 22q11.2 Deletion Syndrome (22q). The absence of a portion of the 22nd chromosome affects every system in the body and is evident in 1 out of ...