Pediatric hyperphosphataemia

Hyperphosphatamia in children is an autosomal recessive genetic disease and is extremely rare. Most people believe that this disease is a disorder of bone tissue metabolism, which is mainly manifested by excessive osteolysis and osteogenesis, which makes ossification insufficiency. The affected areas are commonly found in the skull, tibia, femur, spine, etc. Its characteristics are significantly increased serum alkaline phosphatase, serum calcium and phosphorus are normal.