Warning: Use of undefined constant referer - assumed 'referer' (this will throw an Error in a future version of PHP) in /usr/home/essaywo/public_html/essays on line 102

Warning: Use of undefined constant host - assumed 'host' (this will throw an Error in a future version of PHP) in /usr/home/essaywo/public_html/essays on line 105

Warning: Cannot modify header information - headers already sent by (output started at /usr/home/essaywo/public_html/essays:102) in /usr/home/essaywo/public_html/essays on line 106

Warning: Cannot modify header information - headers already sent by (output started at /usr/home/essaywo/public_html/essays:102) in /usr/home/essaywo/public_html/essays on line 109
Sickle Cell Anemia - Papers Online

Sickle Cell Anemia

Shana Hall
HED
Prof. Frank
Spring 2012

Sickle Cell Anemia

Sickle cell anemia is an inherited chronic disease of the blood. This chronic blood disease is when the body produces abnormal red blood cell shapes. The blood cells become shaped like a crescent or sickle. When this accrues, the blood is unable to produce the right amount of oxygen to the other cells in the body. The sickle cells block blood passageway to the limbs and organs and that lessen the blood flow throughout the body. This causes pain, organ damage, and anemia. Unfortunately, this disease is incurable.
In the sickle cell anemia, the 11[th] chromosome is affected and it causes the disorder in the ...

Want to read the rest of this paper?
Join Essayworld today to view this entire essay
and over 50,000 other term papers

is a 50% (or 1 in 2) chance that any child of theirs also will have SCT, if the child inherits the sickle cell gene from one of the parents. Such children will not have symptoms of SCD, but they can pass SCT on to their children..
These symptoms may not appear until four months after birth. The good thing is that there are treatments that can delay sickle anemia longer. One of the treatments is called hydroxyurea. Hydroxyurea is a drug that decreases the number of nucleotides of defective hemoglobin. Sulphasalazine is another drug. This drug works by reducing the number of "sticky" molecules on red blood cells in sickle-cell anemia. Poloxamer 108 is another drug that shortens the length of the painful episodes in sickle cell anemia. This drug helps by improving blood flow through your vessels to surround the painful areas. The bad thing is that these drug help to cover up the disease and to slow down the extent but it is not a ...

Get instant access to over 50,000 essays.
Write better papers. Get better grades.

Already a member? Login

CITE THIS PAGE:

APA
MLA
Chicago
Turabian

Sickle Cell Anemia. (2012, April 15). Retrieved October 22, 2025, from http://www.essayworld.com/essays/Sickle-Cell-Anemia/100702

"Sickle Cell Anemia." Essayworld.com. Essayworld.com, 15 Apr. 2012. Web. 22 Oct. 2025. <http://www.essayworld.com/essays/Sickle-Cell-Anemia/100702>

"Sickle Cell Anemia." Essayworld.com. April 15, 2012. Accessed October 22, 2025. http://www.essayworld.com/essays/Sickle-Cell-Anemia/100702.

JOIN NOW

Join today and get instant access to this and 50,000+ other essays

PAPER DETAILS

Added: 4/15/2012 12:03:22 AM
Submitted By: shana2585
Category: Diseases & Disorders
Type: Premium Paper
Words: 355
Pages: 2

Save |

Report

SHARE THIS PAPER

SAVED ESSAYS

Save and find your favorite essays easier