Skip to main content
Like
Create new Glog
previous
next
Email share
80 views | 0 likes | 0 reposts
GALACTOSEMIA: A Level One Genetic Disorder...
What is Galactosemia? Galacosemia is a rare genetic disorder that affects one in fifty-five thousand new born infants. It affects the body's ability to break down a food sugar in dairy called galactose.
What are the symptoms and how can you treat it?: Symptoms are kidney failure, enlarged liver, poor growth, and mental retardation. It is treated only by practicing dietary restictions.
How do you get it and how is it diagnosed?: Galactosemia is passed down through an autosomal recessive pattern. It is diagnosed by a prick test to the heel in early infancy.