There are 5 different disorders that result in galactosemia differentiated into three main types. The worst is the Classic form and there are over 180 different mutations associated with this form. The GALT gene is modified by substitution is these examples. The most common one in Caucasian is a single substitution of arginine for glutamine at position 188 on the protein. Another mutation that occurs almost exclusively in individuals of African decent is a single substitution of leucine for serine at position 135.
Some scientists say: -The insulin dependent DDM1, Diabtese mellitus is on chromosome 6 -Type 1 Diabetes was found on chromosome 1q42, and possibly 11 -Type 2 Diabetes on Chromosomes 12 and/or 20
The health condition galactosemia occurs when the body has a deficiency in processing glucose. The condition mostly affects infants and can be life threatening if not treated.
Galactosemia... the word "lactose" in this word should have given you a thoughtless answer.
Galactosemia II is caused by defects in both copies of the gene that codes for an enzyme called galactokinase (GALK). The frequency of occurrence of galactosemia II is about one in 100,000-155,000 births.
yes
Galactosemia is a genetic disorder which is caused by a lack of the GALT enzyme. This is essential in breaking down the milk sugar galactose.
Galactosemia is a condition where infants have trouble digesting lactose to the point where it could harm their organs. People's systems get stronger as people age so older children are no longer affected by the condition.
it was found in 1908 by Von Ruess
the city
sever type1 classic is the most sever type,....... sever type1 (classic): galactosemia is the most sever galactosemic disorder
Many genetic orders such as galactosemia is a disruption in a metabolic pathway. Galactosemia is a disruption in the process of breaking down galactose.