1. Genetics

2. Color Blindness w Occurs more frequently in men w sex-linked (X) w affects light receptors in the eye red/green complete

3. Muscular Dystrophy w Progressive muscle weakness/loss of muscle tissue w Sex - linked w X chromosome w usually begins in early childhood

4. Cystic Fibrosis w Inherit 2 “CF” genes w autosomal disorder w mucus builds up in lungs w 1/2500 people in U.S.

5. Turner Syndrome w A single X chromosome w 1/5000 births w sex organs do not mature w may be shorter than average w puffy hands/feet w neck skin w sterile

6. TURNER’S SYNDROME

7. Klinefelter Syndrome w XXY w 1/2000 births w small testes w sterile w feminine body characteristics w taller than average

8. XYY

9. Down Syndrome w Trisomy 21 w broad, flat face w upslanted eyes w mental retardation w 1/700 births in U.S. w The older you are the greater your risk!

10. DOWN SYNDROME

11. Fragile X Syndrome w Abnormal X chromosome w mental retardation w 1/2500 males w 1/1500 females

13. PATAU SYNDROME TRISOMY 13

14. PATAU

15. Dwarfism w Average size trunk with short arms and legs typical

16. BALDNESS w Sex-Influenced traits. w More common in men than women. w Not exactly sure where this trait resides? w Men get it if homozygous recessive bb or heterozygous Bb! Women only get it if they are homozygous recessive bb.

17. HUNTINGTON DISEASE w Dominant Trait. w Shows up in the thirties and forties, damage to nervous system begins. w Leads to mental retardation and loss of muscle control w Located on the 4th chromosome

18. SICKLE CELL ANEMIA w A disorder where the red blood cells are in the shape of a sickle. w Co-dominant disorder w heterozygous=carriers w Mostly found in people with african heritage. w Reason? Malaria, SCA is partially resistant.

19. HEMOPHILIA w Sex-linked disorder w Recessive allele w bleeder’s disease w Clotting factor is missing. w 1:10,000 males w 1:100,000,000 females w treatment-injecting clotting factors

20. SPINA BIFIDA w When vertebrae in your spinal cord fail to develop and leaves a space causing damage to the nervous system

22. Cri Du Chat w 1: 50,000 w deletion on chromosome 5 w abnormal larynx development w cry of the cat w Low birth weight w Respiratory problems