X-linked hypophosphatemia

X-linked hypophosphatemia is a genetic disorder that affects how the body handles phosphate, a mineral vital for healthy bones and teeth. Due to a gene mutation, the body loses too much phosphate through the kidneys, leading to weak, soft bones that may cause deformities, fractures, or delayed growth. It commonly runs in families and usually starts showing symptoms in childhood. Treatment often involves supplements and medications to improve phosphate levels and support normal bone development. Early diagnosis and management are important to help reduce complications and improve quality of life.