NF1 and pseudohypoparathyroidism type 1A: The causality of the two identified molecular abnormalities is unclear in this case, and any association may be purely speculative, but the heterogeneity of AHO does not dilute the possibility of a link between the 17q11.2 and the clinical features in this case, and it may be worth considering testing other cases of NF1 microduplication for PTH levels.