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Genetics
Huntington’s disease is an autosomal dominant inheritance. It is a neurodegenerative condition which damages brain cells, resulting in the person’s diminish ability to speak, walk, talk and swallow.
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What terms describe autosomal?
2 points
Non-sex chromosome
Sex chromosome
Chromosome 4
Chromosome X and Y
What are all the possible genotype of a child with Huntington disease, if the mother is homozygous dominant (HH) and the father is heterozygous (Hh)?
3 points
Hh only.
HH, Hh or hh
Hh or HH
HH only
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