Which of the following is NOT an assessment data point for DiGeorge's Syndrome?

DiGeorge's Syndrome, also known as 22q11.2 deletion syndrome, is characterized by a range of clinical features resulting from a microdeletion on chromosome 22. Among the common assessment data points for this condition are recurrent infections, cardiac abnormalities, and cleft palate.

Recurrent infections occur due to the underdevelopment of the thymus gland, leading to immunodeficiency. Cardiac abnormalities are prevalent, with congenital heart defects being frequently seen in individuals with DiGeorge's Syndrome. Cleft palate is another notable feature linked to this genetic condition and can often be a significant aspect of the clinical presentation.

In contrast, hypercalcemia is not typically associated with DiGeorge's Syndrome. Instead, individuals with this syndrome often experience hypoparathyroidism, which leads to low calcium levels (hypocalcemia) rather than high levels. This distinction is crucial for understanding the pathophysiology of DiGeorge's Syndrome and its related health implications.