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Galactosemia is a condition that affects how the body digests the sugar galactose. The most common form of galactosemia, type I, is the most severe, and it results from mutations within the GALT gene, which encodes for an enzyme that processes galactose. Galactosemia is inherited in an autosomal recessive pattern.Imagine that your friend Mary has normal metabolism, but that her brother John has galactosemia. Mary and John's parents, Patricia and Les, are unaffected, although their maternal grandmother, Jean, also had the condition. If wild-type GALT is designated as G and the recessive allele is designated as g, determine the genotypes of the following individuals. Drag a genotype to each individual in the pedigree. Labels may be used more than once or not at all.


A newborn daughter has a one in eight chance of developing the illness. Individuals with galactosemia are unable to fully metabolize galactose, a sugar found in milk. This leads to the accumulation of galactose-derived compounds in various bodily organs, such as the eyes, kidneys, liver, and brain, causing harm to the individual. Galactosemia is caused by mutations in the GALT gene, which results in a deficiency of the GALT enzyme. This abnormal buildup of molecules associated with galactose in different bodily organs leads to the clinical manifestations of galactosemia, including its signs, symptoms, and physical findings. Galactosemia is a metabolic disease that some newborns are born with, and it is caused by a malfunction of the enzymes responsible for breaking down galactose. Elevated levels of galactose are detected in newborns diagnosed with galactosemia. For more information about galactosemia, please visit brainly.com/question/14600502 #SPJ4.