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21 February, 17:45

Question

Type your response in the box.

Galactosemia is an inherited genetic condition. Children with this condition cannot break down the sugar galactose,

which is part of lactose. Based on the pedigree chart, is this condition a dominant or a recessive disorder? Explain

your reasoning.

unaffected

carrier

father

unaffected

carrier

mother

+3
Answers (1)
  1. 21 February, 19:40
    0
    Galactosemia is a recessive disorder.

    Explanation:

    the dominant trait for digestion is normal digestion (G), and recessive would then be galactosemia (g).
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