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Genetic Disorders Clip 49
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Huntington’s Disease 49 1/2
Huntington's disease (Huntington's chorea) is a progressive, degenerative disease that causes certain nerve cells in your brain to waste away. As a result, you may experience uncontrolled movements, emotional disturbances and mental deterioration. The disorder was documented in 1872 by American physician George Huntington. Fatal----ages:30-60 Dominant Allele 49 1/2
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Colorblindness Sex-linked trait
Gene for color vision located on the X chromosomes. Males are more likely to have colorblindness because they have only one X chromosome 50
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What do you see? What do you see? 51
The individual with normal color vision will see a 5 revealed in the dot pattern. An individual with Red/Green (the most common) color blindness will see a 2 revealed in the dots. 51
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TEST 53
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Down Syndrome Sister chromatid DO NOT separate during Meiosis.
3 copies of chromosome #21. Sister chromatid DO NOT separate during Meiosis. (or homologues fail to separate ) Nondisjunction 54
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Nondisjunction Sister chromatid DO NOT separate during Meiosis.
Or homologues fail to separate during Meiosis.
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Down Syndrome - Trisomy 21
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Nondisjunction 57
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Down Syndrome 58
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Cystic Fibrosis 59 CF is caused by a recessive allele on chromosome #7. Deletion of 3 bases. Affects the body's respiratory and digestive systems. Asian & African- less likely to have.
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Hemophilia 60 Recessive allele Sex-liked Trait
Located on the X chromosome Missing a protein necessary for blood clotting Major bleeding from minor cuts. 60
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People who carry the tendency to have sickle cell anemia are less likely to die from malaria.
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Tay-Sachs Harmful quantities of a fatty acids accumulate in the nerve cells of the brain. Caused by insufficient activity of an enzyme called beta-hexosaminidase A that catalyzes the biodegradation of acidic fatty materials Fatal 62 1/2
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