Hypophosphatasia

Hypophosphatasia is a rare hereditary disease associated with a disorder of phosphate metabolism, caused by a mutation in the gene encoding the enzyme hydroxylase-phosphate dehydrogenase (HPS1), which leads to a decrease in enzyme activity. With this disease, phosphorus metabolism is disrupted, which leads to its excessive accumulation in the blood and tissues.

Hypophosphatasia is an inherited disease caused by a deficiency of lysyl oxidase. It occurs due to the absence or deficiency of the enzyme lysyl oxidase in the body, which leads to disruption of the metabolism of minerals such as calcium and phosphorus.

Hypophosphiasia is a genetic disease characterized by impaired phosphorus metabolism. Its deficiency can lead to a variety of health problems, including muscle weakness, heart problems, bone loss, and even death. Phosphate deficiency can lead to serious health consequences. To treat hypophosphatia, special diets containing