Consequent to the GNAS gene being subject to imprinting, AHO patients show variable hormone unresponsiveness: those with mutations on maternally inherited alleles manifest multiple hormone resistance (PTH, TSH, gonadotropins, GHRH, and glucagon) leading to PHP type 1A, while patients with mutations on paternally inherited alleles have phenotypic features of AHO without hormonal resistance (pseudopseudoparathyroidism) in consequence to Gsα expression from the paternal allele being normally suppressed because of imprinting in hormone-target tissues (6,7). Here, GCG is linked to pseudohypoparathyroidism type 1A.