Genetic Disorders: Decoding the Blueprint of Human Identity
Introduction and Definition Albright’s Hereditary Osteodystrophy, often abbreviated as AHO, is a complex, rare, genetic health problem characterized by a distinct set of physical and biochemical abnormalities. Fundamentally, AHO is classified as a form of Pseudohypoparathyroidism (PHP), specifically PHP Type 1A. While the clinical presentation closely mimics true hypoparathyroidism, exhibiting symptoms associated with low calcium […]