1) Pick either an autosomal recessive or dominant genetic disorder/disease and briefly discuss the associated symptoms.
2) Discuss what gene(s) is/are affected by this disorder and how it compromises the body.
3) What individuals are affected by this disorder (on the chromosomal level)? What individuals are not affected by this disorder? Briefly include who are carriers, if applicable.
4) Briefly discuss screening or diagnostic tools that can be used to detect this disorder.
5) Briefly discuss treatment options for this disorder.