Galactosemia is a rare autosomal recessive condition with the most common form, Classic Galactosemia (CG) or Type I Galactosemia, being a result of galactose-1-phosphate uridylyltransferase (GALT) gene mutation that occurs in 1/16,000 to 1/60,000 births worldwide [1, 2], and approximately 1/50,000 births in the US [2]. Here, GALT is linked to classic galactosemia.