De Vries Syndrome

De Vries syndrome is a rare hereditary disease that is characterized by developmental delay and various mental illnesses. This disease is unknown to the general public because it affects only a small number of people living in certain areas of Israel and Western Europe. However, as the diagnosis becomes more common, it is necessary to address existing problems and try to solve them without delaying the matter.

De Vries syndrome is named after the famous geneticist who noticed this phenomenon and began to study it. The term appeared in 2015 after the publication of his research results. De Vries believes that it is associated with genetic mutations that are transmitted at the genetic level and lead to various diseases. To date, the syndrome has not been associated with specific genetic changes, so more research in gene therapy and genetics is required to identify the causes.

DeVry syndrome is a term that refers to a group of diseases associated with impaired bone maturation in children. The syndrome was named after pediatrician DeVries, who first described it in 1955. De Vries noticed that in some children the process of bone development stops at a certain stage of growth and