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People with Waardensburg have a normal life expectancy. Prenatal tests are possible for Parents to test for Waardenburg Syndrome, although they are not recommended due to the high risk of miscarriage.

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c. 1.Heterochromia- different colored pigments of eyes
2. Constipation
3. Deafness, hearing impairments
4. Partial Albinism
5. Wide set eyes
6. Cleft lip
7. White patch of hair or early graying of the hair
8. Possible slight decrease in intellectual function
9. Difficulty completely straightening joints
d.  There is no specific treatment. Special diets and medicines to keep the bowel moving are prescribed to those patients who have constipation. (Medicine 1)
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There are multiple names for Waardenburg syndrome. They include Klein-Waardenburg syndrome and Waardenburg-Shah syndrome. More precisely, the EDN3 gene is located from base pair 59,300,424 to base pair 59,325,992 on chromosome 20. (NORD 1)

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B = Waardenburgs
b = Normal
(Mutations 1)

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Rarity is between 1/42000-50000 people. All ages and sexes are affected equally. I would show them all of the possible side affects of the disease and show them the odds of their child having this defect. (Genetics 1)

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Waardenburg Syndrome is a polygenic mutation that is purely based on genetic factors alone. Waardensburg Syndrome arose from genetic mutations. It is an autosomal dominant trait. (Wikipedia 1)

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"Waardenburg Syndrome: MedlinePlus Medical Encyclopedia." U.S National Library of                Medicine. U.S. National Library of Medicine, n.d. Web. 26 Feb. 2016.
"Waardenburg Syndrome - NORD (National Organization for Rare Disorders)." NORD                 (National Organization for Rare Disorders). N.p., n.d. Web. 26 Feb. 2016.
"Waardenburg Syndrome." WebMD. WebMD, n.d. Web. 26 Feb. 2016.
Waardenburg Syndrome." Genetics Home Reference. N.p., n.d. Web. 26 Feb. 2016.
Wikipedia. Wikimedia Foundation, n.d. Web. 26 Feb. 2016.
"Genetics of Waardenburg Syndrome." : Overview, Gene Mutations. N.p., n.d. Web. 26                   Feb. 2016.

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a. Waardenburg syndrome, Klein-Waardenburg syndrome; Waardenburg-Shah syndrome
b. More precisely, the EDN3 gene is located from base pair 59,300,424 to base pair 59,325,992 on chromosome 20.
c. 1.Heterochromia- different colored pigments of eyes
2. Constipation
3. Deafness, hearing impairments
4. Partial Albinism
5. Wide set eyes
6. Cleft lip
7. White patch of hair or early graying of the hair
8. Possible slight decrease in intellectual function
9. Difficulty completely straightening joints
d.  There is no specific treatment. Special diets and medicines to keep the bowel moving are prescribed to those patients who have constipation.
e. Normal life expectancy
f. Prenatal tests are possible for Parents to test for Waardenburg Syndrome, although they are not recommended due to the high risk of miscarriage.