CASR and 22q11.2 deletion syndrome: Other etiologies included primary idiopathic disease (n = 7), autoimmune polyglandular syndrome type 1 (n = 2), autosomal dominant hypocalcemia (activating mutation of the calcium-sensing receptor) (n = 1), hypoparathyroidism, sensorineural deafness, and renal disease (also known as Barakat syndrome) (n = 1), and DiGeorge syndrome (n = 1).