Galactosemia

Essay specific features

 

Issue:

Science

 

Written by:

William F

 

Date added:

September 22, 2014

 

Level:

 

Grade:

A

 

No of pages / words:

5 / 1267

 

Was viewed:

7095 times

 

Rating of current essay:

 
Essay content:

Their structure is determined by their coding on DNA. Inborn errors of metabolism, like the one seen in galactosemia, are caused by defective genes. Galactosemia is an inherited metabolic disorder in which the transformation of galactose to glucose is blocked, allowing galactose to increase to toxic levels in the body (Chung 1997)...
displayed 300 characters

Custom written essay

All essays are written from scratch by professional writers according to your instructions and delivered to your email on time. Prices start from $10.99/page

Order custom paper

Full essays database

You get access to all the essays and can view as many of them as you like for as little as $28.95/month

Buy database access

Order custom writing paper now!

  • Your research paper is written
    by certified writers
  • Your requirements and targets are
    always met
  • You are able to control the progress
    of your writing assignment
  • You get a chance to become an
    excellent student!

Get a price guote

 
 

Galactose epimerase, the enzyme in the liver that is required to break down galactose, is deficient in galactosemia patients ("Galactosemia" 1995 and Wohlers, Christacos, and Harreman 1999). This enzyme works as a catalyst to speed up the breakdown of galactose. When there is a deficiency of this enzyme, the body cannot metabolize galactose as quickly as needed, causing a toxic buildup (Olendore, Jenyan, and Bayden 1999)...
displayed 300 characters

General issues of this essay:

Related essays:

x
Services