Question

What is Galactosemia ?​

Answer 1

Here is Your Answer...

⚡Its an inborn [congenital] error of galactose metabolism resulting from the absence of Uridyl Transferase enzyme in the liver.

Transferase enzyme in the liver.

⚡This enzyme converts glactose into glucose.

Transferase enzyme in the liver.

⚡This enzyme converts glactose into glucose.

⚡Galactosseinia is characterized by high concentration of galactose in the blood that cause mental retardation and damage..

Answer 2

☣☣Galactosemia: An inherited disorder of galactose metabolism that occurs in newborns and can result in damage to the liver, brain, kidneys, and other organs in infants due to the accumulation of galactose derivatives in the body.

☣☣Galactosemia: An inherited disorder of galactose metabolism that occurs in newborns and can result in damage to the liver, brain, kidneys, and other organs in infants due to the accumulation of galactose derivatives in the body.☣☣Galactosemia is inherited as an autosomal recessive trait.

☣☣Galactosemia: An inherited disorder of galactose metabolism that occurs in newborns and can result in damage to the liver, brain, kidneys, and other organs in infants due to the accumulation of galactose derivatives in the body.☣☣Galactosemia is inherited as an autosomal recessive trait. ☣☣Galactosemia is due to deficient activity of the enzyme galactose-phosphate uridyltransferase (GALT).

☣☣Galactosemia: An inherited disorder of galactose metabolism that occurs in newborns and can result in damage to the liver, brain, kidneys, and other organs in infants due to the accumulation of galactose derivatives in the body.☣☣Galactosemia is inherited as an autosomal recessive trait. ☣☣Galactosemia is due to deficient activity of the enzyme galactose-phosphate uridyltransferase (GALT). ☣☣Molecular testing for the gene that produces GALT permits carrier detection, genetic counseling, and prenatal diagnosis.