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Galactosemia: A Rare Milk Sugar Disorder
Galactosemia is a rare congenital disorder which affects the body's inability to convert galactose into glucose. Galactose is a type of sugar, which is a breakdown product of lactose. Lactose is found in milk and milk products, including breast milk. Given that the galactose can not be broken down, it builds up in the body and acts as a poison that can cause serious damage to it‘s carrier("galactosemia"). "As milk is important to a baby's diet, early diagnosis is essential to avoid lifelong problems from this potentially fatal disorder "(Chung). This research paper provides information about the genetic part of Galactosemia, the cause, symptoms, diagnosis, treatment.

The first trace of information that was brought to light about galactosemia was in 1908 by Von Ruess. He composed an article of his findings in an infant with many of the symptoms we now relate to galactosemia. This work has widely been accepted by scientists as the......

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Approximate Word Count: 795
Approximate Pages: 4 (250 words per double-spaced page)

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