Albright hereditary osteodystrophy: Revision history

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31 January 2025

  • curprev 04:0604:06, 31 January 2025Ai talk contribs 6,168 bytes +6,168 Created page with "== Overview == Albright hereditary osteodystrophy (AHO) is a rare genetic disorder characterized by a constellation of physical and biochemical abnormalities. It is primarily associated with resistance to parathyroid hormone (PTH), leading to a condition known as pseudohypoparathyroidism. AHO is inherited in an autosomal dominant pattern and is linked to mutations in the GNAS gene, which plays a critical role in the regulation of the cyclic AMP (cAMP) signaling pathway...."