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A Glimpse Into Albinism

Physiological changes have been taking place ever since the first organisms appeared on Earth. These changes have led to the tremendous variation we see in modern humans today. To try and explain these differences, scientists use human fossil remains as well as other primate remains to trace evolutionary similarities. Important fields of study such as anthropology, biology, primatology and paleoanthropology also help in the attempt to adequately explain human anatomical differences and their reasons for occurring (Jolly 9-10). A commonly misunderstood and extremely interesting example of human variation is albinism.

Nearly one in every 17,000 people has some form of albinism and the United States has reported over 18,000 such cases. Sufferers of albinism exhibit very little or have no pigment in their skin, eyes and hair. Strangely enough, parents of those who have this condition in most cases have hair, eye and skin color that are typical of their race and it is rare for there to be a family history of it (Haefemeyer 55-56). Sufferers of albinism have inherited a malfunctioned and altered copy of their parent’s gene that codes for melanin production. This is most commonly known as autosomal r

. . .
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Albinism Physiological, Renaissance Europe, Nystagmus Witkop, Lastly DNA, OCA OC, OCA Witkop, melanin pigment, sufferers albinism, lack melanin, skin eyes hair, skin eyes, eye brain, form albinism, nerve connections, albinism melanin, associated albinism, albinism minimize,
Approximate Word count = 1383
Approximate Pages = 6 (250 words per page double spaced)

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