Hereditary Fructose Intolerance

Version	Summary	Created by	Modification	Content Size	Created at	Operation
1		Camila Xu	+ 489 word(s)	489	2020-12-15 07:26:33

This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/condition/hereditary-fructose-intolerance

Hereditary fructose intolerance is a condition that affects a person's ability to digest the sugar fructose. Fructose is a simple sugar found primarily in fruits.

genetic conditions

1. Introduction

Affected individuals develop signs and symptoms of the disorder in infancy when fruits, juices, or other foods containing fructose are introduced into the diet. After ingesting fructose, individuals with hereditary fructose intolerance may experience nausea, bloating, abdominal pain, diarrhea, vomiting, and low blood sugar (hypoglycemia). Affected infants may fail to grow and gain weight at the expected rate (failure to thrive).

Repeated ingestion of fructose-containing foods can lead to liver and kidney damage. The liver damage can result in a yellowing of the skin and whites of the eyes (jaundice), an enlarged liver (hepatomegaly), and chronic liver disease (cirrhosis). Continued exposure to fructose may result in seizures, coma, and ultimately death from liver and kidney failure. Due to the severity of symptoms experienced when fructose is ingested, most people with hereditary fructose intolerance develop a dislike for fruits, juices, and other foods containing fructose.

Hereditary fructose intolerance should not be confused with a condition called fructose malabsorption. In people with fructose malabsorption, the cells of the intestine cannot absorb fructose normally, leading to bloating, diarrhea or constipation, flatulence, and stomach pain. Fructose malabsorption is thought to affect approximately 40 percent of individuals in the Western hemisphere; its cause is unknown.

2. Frequency

The incidence of hereditary fructose intolerance is estimated to be 1 in 20,000 to 30,000 individuals each year worldwide.

3. Causes

Mutations in the ALDOB gene cause hereditary fructose intolerance. The ALDOB gene provides instructions for making the aldolase B enzyme. This enzyme is found primarily in the liver and is involved in the breakdown (metabolism) of fructose so this sugar can be used as energy. Aldolase B is responsible for the second step in the metabolism of fructose, which breaks down the molecule fructose-1-phosphate into other molecules called glyceraldehyde and dihydroxyacetone phosphate.

ALDOB gene mutations reduce the function of the enzyme, impairing its ability to metabolize fructose. A lack of functional aldolase B results in an accumulation of fructose-1-phosphate in liver cells. This buildup is toxic, resulting in the death of liver cells over time. Additionally, the breakdown products of fructose-1-phosphase are needed in the body to produce energy and to maintain blood sugar levels. The combination of decreased cellular energy, low blood sugar, and liver cell death leads to the features of hereditary fructose intolerance.

4. Inheritance

This condition is inherited in an autosomal recessive pattern, which means both copies of the gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition.

5. Other Names for This Condition

ALDOB deficiency
aldolase B deficiency
fructose aldolase B deficiency
fructose intolerance
fructose-1,6-biphosphate aldolase deficiency
fructose-1-phosphate aldolase deficiency
fructosemia

References

Bouteldja N, Timson DJ. The biochemical basis of hereditary fructoseintolerance. J Inherit Metab Dis. 2010 Apr;33(2):105-12. doi:10.1007/s10545-010-9053-2.
Coffee EM, Yerkes L, Ewen EP, Zee T, Tolan DR. Increased prevalence of mutant null alleles that cause hereditary fructose intolerance in the Americanpopulation. J Inherit Metab Dis. 2010 Feb;33(1):33-42. doi:10.1007/s10545-009-9008-7.
Esposito G, Vitagliano L, Santamaria R, Viola A, Zagari A, Salvatore F.Structural and functional analysis of aldolase B mutants related to hereditaryfructose intolerance. FEBS Lett. 2002 Nov 6;531(2):152-6.
Santer R, Rischewski J, von Weihe M, Niederhaus M, Schneppenheim S, BaerlocherK, Kohlschütter A, Muntau A, Posselt HG, Steinmann B, Schneppenheim R. Thespectrum of aldolase B (ALDOB) mutations and the prevalence of hereditaryfructose intolerance in Central Europe. Hum Mutat. 2005 Jun;25(6):594.

©Text is available under the terms and conditions of the Creative Commons-Attribution ShareAlike (CC BY-SA) license; additional terms may apply. By using this site, you agree to the Terms and Conditions and Privacy Policy.

Upload a video for this entry

Information

Subjects: Genetics & Heredity

Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :

Camila Xu

View Times: 601

Entry Collection: MedlinePlus

Update Date: 23 Dec 2020

Table of Contents

Video Upload Options

Confirm

1. Introduction

2. Frequency

3. Causes

4. Inheritance

5. Other Names for This Condition

References

Video Upload Options

Confirm

1. Introduction

2. Frequency

3. Causes

3.1. The gene associated with Hereditary fructose intolerance

4. Inheritance

5. Other Names for This Condition

References