StudentShare
Contact Us
Sign In / Sign Up for FREE
Search
Go to advanced search...

The genetic basis of glucose-6-phosphate dehydrogenase (G6PD) deficiency - Essay Example

Cite this document
Summary
G6PD deficiency affects more than four hundred million people around the world. Its prevalence around the world has marked similarity to that of malaria, which has led to…
Download full paper File format: .doc, available for editing
GRAB THE BEST PAPER98.7% of users find it useful
The genetic basis of glucose-6-phosphate dehydrogenase (G6PD) deficiency
Read Text Preview

Extract of sample "The genetic basis of glucose-6-phosphate dehydrogenase (G6PD) deficiency"

Download file to see previous pages

008, pp.64, define G6PD deficiency as “an X-linked, hereditary genetic defect due to mutations in the G6PD gene, which cause functional variants with many biochemical and clinical phenotypes”. Most of the mutations are single base changes that result in amino acid substitutions. G6PD deficiency presents itself clinically in the form of acute haemolytic anaemia (Capellini & Fiorelli, 2008). The gene responsible for the production of the enzyme G6PD is the G6PD gene G6PD is the catalyst responsible for oxidising glucose-6-phosphate to 6-phosphogluconate, while at the same time it is also responsible for the reduction of the oxidised form of nicotanamide adenine dinucleotide phosphate (NADP+) to nicotinamide adenine dinucleotide phosphate (NADPH).

This function of G6PD in the production of NADPH is important, as it is NADPH that plays a role as a cofactor in many biosynthetic reactions and maintaining glutathione in its reduced form (Carter & Gross, 2008). Reduced glutathione functions as a scavenger within cells, removing the dangerous oxidative metabolites in the cells. In addition with assistance from the enzyme glutathione peroxidase, it neutralizes hydrogen peroxide, which is harmful to the cell, by converting it to water. G6PD and its role in the production of NAPDH is important to red blood cells, as NAPDH is the sole contributor of protection to the red blood cells against oxidative stresses, The importance of G6PD to the red blood cells lies in it being the sole source of NAPDH and the protection NAPDH offers the red blood cells (Carter & Gross, 2008).

The G6PD gene that is responsible for the enzyme Glucose-6-Phosphate Dehydrogenase is found on the terminal region of the long arm of the X chromosome (Xq28), at a distance of less than 2 centi-Morgan centrometric to the Factor VIII gene. G6PD deficiency is a genetic condition, wherein the molecular grounds for the disease stems from mutations in the G6PD locus at Xq28. The length of the gene is 18

...Download file to see next pages Read More
Cite this document
  • APA
  • MLA
  • CHICAGO
(“The genetic basis of glucose-6-phosphate dehydrogenase (G6PD) Essay”, n.d.)
The genetic basis of glucose-6-phosphate dehydrogenase (G6PD) Essay. Retrieved from https://studentshare.org/miscellaneous/1551680-the-genetic-basis-of-glucose-6-phosphate-dehydrogenase-g6pd-deficiency
(The Genetic Basis of Glucose-6-Phosphate Dehydrogenase (G6PD) Essay)
The Genetic Basis of Glucose-6-Phosphate Dehydrogenase (G6PD) Essay. https://studentshare.org/miscellaneous/1551680-the-genetic-basis-of-glucose-6-phosphate-dehydrogenase-g6pd-deficiency.
“The Genetic Basis of Glucose-6-Phosphate Dehydrogenase (G6PD) Essay”, n.d. https://studentshare.org/miscellaneous/1551680-the-genetic-basis-of-glucose-6-phosphate-dehydrogenase-g6pd-deficiency.
  • Cited: 0 times

CHECK THESE SAMPLES OF The genetic basis of glucose-6-phosphate dehydrogenase (G6PD) deficiency

Errors of metabolism (newborn screening)

Topic: Errors Of Metabolism (Newborn Screening) Date: Background of Disease Medium chain acyl Co A dehydrogenase deficiency (MCADD) is one of fatty acid oxidation disorder affecting fatty acid oxidation, thus preventing the conversion of fats to energy.... (Wilson, 1999) Variation in Symptoms and Prognosis The deficiency of this enzyme is characterised by symptoms such as hypoketotic hypoglycaemia, vomiting (Egidio RJ, 1989) and hypotonia progressing to coma....
4 Pages (1000 words) Essay

The Biochemical Cause for the Defective Muscle Glycogen Synthesis

In an effort to diagnose his condition, you examined mitochondria in muscle cells obtained from a biopsy and detect a deficiency in oxidative metabolism.... The paper describes hypotonia, poor feeding.... The patient's mitochondria consumed oxygen normally when incubated with pyruvate and malate....
5 Pages (1250 words) Essay

Hemolytic Anemia in G6PD Patients

Belsey (1973) explained that the g6pd deficiency has got a sex-linked inheritance.... hellip; The author states that the rigorousness of enzyme deficiency often does not associate well with the clinical severity of genetic diseases.... Thus, some G6PD variants linked with rigorous enzyme deficiency, such as Union and Markham, cause no hemolytic problem, while some variants related to the less severe deficiency.... s are the most commonly and most severely damaged population of cells due to the deficiency of this enzyme....
4 Pages (1000 words) Case Study

Malate Dehydrogenase Isoenzymes

The lab report "Malate dehydrogenase Isoenzymes" points out that This experiment examined the localization of three enzymes within liver cells.... The enzymes being examined were malate dehydrogenase (MDH), lactate dehydrogenase (LDH) and succinate dehydrogenase (SDH)....
5 Pages (1250 words) Lab Report

What is Anemia

He pointed out signs such as paleness of skin color and general weakness of the patient who had… The principle was understood to be a decrease in the red blood cells that ultimately caused death of the patient (Gale). Being the most widespread form of anemia, this is primarily caused due to deficiency of iron in the body-either due to imbalanced diet Furthermore, deficiency of vitamins such as B-12, an integral component for formation of healthy red blood cells, also cause vitamin related anemia (American Society of Hematology)....
6 Pages (1500 words) Research Paper

Utilize a genomic case study (other options)

In 2013, a child came into the hospital suffering from an inherited, rare, and undiagnosed metabolic disorder, MCADD or medium chain acyl-coenzyme A dehydrogenase deficiency and, although he had seemed healthy at birth, failure to eat for too long made him vary sick and he… For children diagnosed early with the genetic disorder, it is imperative that they avoid going for too long without food and, had this child undergone genomic newborn screening, this would have been realized and his parents able to take precaution and save his ewborn and prenatal genomic screening, started in US hospitals with voluntary tests for PKU before it was made mandatory, especially as a response to lobbying by advocates for child rights....
4 Pages (1000 words) Essay

New Loci for Genetic Resistance to Malaria in Humans

sickle cell hemoglobin variant (Hb-S) and glucose-6-phosphate dehydrogenase (G6PDH).... tudies on the genetic make-up of the human body have been enhanced by the construction of a complete human genome.... This work "New Loci for genetic Resistance to Malaria in Humans" describes the nature of various disease conditions and susceptibility to the conditions in relation to the body's genetic make-up.... The author outlines the potential of genome-wide studies in the identification of genetic linkages that infer protection against infectious diseases such as malaria....
6 Pages (1500 words) Essay

Genetic Basis of Diabetes

This report "genetic basis of Diabetes" focuses on a heterogeneous disorder that has characteristics of persistent hyperglycemia.... ype 2 diabetes genetic basis is known to be complicated to resolve.... In this case, type 2 diabetes is a relative disease but not insulin deficiency....
6 Pages (1500 words) Report
sponsored ads
We use cookies to create the best experience for you. Keep on browsing if you are OK with that, or find out how to manage cookies.
Contact Us