Is hunter syndrome a shortened form of huntington's disease ? - Hunter syndrome

Hunter Syndrome            Hunter syndrome is one type of a metabolic disorder called mucopolysaccharidosis that is inherited. This is also referred as MPS II. MPS IIA and MPS IIB are two subtypes of Hunter syndrome and their symptoms are different.More...

History Of Hunter Syndrome

History Of Hunter Syndrome

Hunter Syndrome is a genetic disorder caused by the deficiency of an enzyme called iduronate-2-sulfatase (12S). This is a condition which generally affects males.  This disease was first discovered in 1917 when two brothers were found to be having this disorder. This was first described by Charles A. Hunter who was a Professor of Medicine in Canada. This disease has been named after him.More...

 

Hunter Syndrome Treatment

Hunter Syndrome Treatment

Hunter syndrome is a hereditary disease. There is a breakdown of a mucopolysaccharide where a chemical that is widely distributed in the body outside of cells gets defected. Deficiency of I2S or technically speaking, lack of the enzyme iduronate sulfatase is the main reason for this metabolic abnormality that leads to Hunter syndrome. Without this enzyme, mucopolysaccharidosis collected in various body tissues, cause damage.More...

 

Is Hunter Syndrome A Shortened Form Of Huntington's Disease ?

Is Hunter Syndrome A Shortened Form Of Huntington's Disease

Hunter syndrome is a rare disorder, which is caused by deficiency of an enzyme called iduronate sulfatase. This enzyme is necessary to break down the complex sugar produced in the body. While Huntington’s disease is a genetic disorder where there is gradual development of involuntary muscles which affect the hands, feet, trunk and the face. There may also be progressive deterioration of memory. It is caused by a defective gene, and is hereditary.More...