Fructose Intolerance, Hereditary

Fructose Intolerance, Hereditary

National Organization for Rare Disorders, Inc.

Important

It is possible that the main title of the report Fructose Intolerance, Hereditary is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.

Synonyms

  • Fructose-1-Phosphate Aldolase Deficiency
  • Fructosemia

Disorder Subdivisions

  • None

General Discussion

There are three inherited disorders of fructose metabolism that are recognized and characterized. Essential fructosuria, is a mild disorder not requiring treatment, while Hereditary fructose intolerance (HFI) and Hereditary fructose-1,6-biphosphatase deficiency (HFBP) are treatable and controllable but must be taken seriously.



Hereditary Fructose Intolerance (HFI) is an inherited inability to digest fructose (fruit sugar) or its precursors (sugar, sorbitol and brown sugar). This is due to a deficiency of activity of the enzyme fructose-1-phosphate aldolase, resulting in an accumulation of fructose-1-phosphate in the liver, kidney, and small intestine. Fructose is a naturally occurring sugar that is used as a sweetener in many foods, including many baby foods. This disorder can be life threatening in infants and ranges from mild to severe in older children and adults.



People who have HFI usually develop a strong dislike for sweets and fruit. After eating foods containing fructose, they may experience such symptoms as severe abdominal pain, vomiting, and low blood sugar (hypoglycemia).



Early diagnosis is important because, while most people who have HFI can lead normal lives if they adopt a fructose-free diet. If left untreated however, the condition can lead to permanent physical harm, including especially, serious liver and kidney damage.

Symptoms

Soon after fructose is added to the diet of an infant with HFI, symptoms become apparent. These may include prolonged vomiting, failure to thrive, jaundice and growth retardation. There may be occasional episodes of unconsciousness. Other symptoms include enlargement of the liver and frequently cirrhosis, and a tendency towards gastrointestinal bleeding because of deficiency of clotting factors. There are decreased levels of glucose and phosphate in the blood and increased levels of fructose in the blood and urine.



Patients with Hereditary Fructose Intolerance usually develop a strong dislike for sweets and fruit. Although infants may exhibit growth delays and even experience malnutrition, there is no intellectual impairment.



It is very important to recognize the intolerance early to avoid damage to the liver, kidney, and small intestine.

Causes

Studies of families in which HFI occurs leads geneticists to believe that the disorder is inherited as an autosomal recessive trait, The responsible gene has been mapped to the long arm (q) of chromosome 9 at gene map locus 9q22.3.



Chromosomes, which are present in the nucleus of human cells, carry the genetic information for each individual. Human body cells normally have 46 chromosomes. Pairs of human chromosomes are numbered from 1 through 22 and the sex chromosomes are designated X and Y. Males have one X and one Y chromosome and females have two X chromosomes. Each chromosome has a short arm designated "p" and a long arm designated "q". Chromosomes are further sub-divided into many bands that are numbered. For example, "chromosome 9q22.3" refers to band 22.3 on the long (q) arm of chromosome 9. The numbered bands specify the location of the thousands of genes that are present on each chromosome.



Genetic diseases are determined by the combination of genes for a particular trait that are on the chromosomes received from the father and the mother.



Recessive genetic disorders occur when an individual inherits the same abnormal gene for the same trait from each parent. If an individual receives one normal gene and one gene for the disease, the person will be a carrier for the disease, but usually will not show symptoms. The risk for two carrier parents to both pass the defective gene and, therefore, have an affected child is 25% with each pregnancy. The risk to have a child who is a carrier like the parents is 50% with each pregnancy. The chance for a child to receive normal genes from both parents and be genetically normal for that particular trait is 25%. The risk is the same for males and females.



All individuals carry 4-5 abnormal genes. Parents who are close relatives (consanguineous) have a higher chance than unrelated parents to both carry the same abnormal gene, which increases the risk to have children with a recessive genetic disorder.

Affected Populations

Hereditary Fructose Intolerance may be diagnosed at birth or shortly thereafter when the infant is weaned. Like other autosomal disorders it is equally distributed among males and females. Estimates of the incidence of the disorder range widely from 1:10,000 to 1:100,000 births.

Standard Therapies

Diagnosis

A diagnosis of HFI can be definitively confirmed by either of two tests: an enzyme assay, requiring a liver biopsy, to determine the level of aldolase activity or a fructose tolerance test in which the patient's response to intravenous fructose feeding is carefully monitored. It should be carefully noted, however, that each of these tests carries with it a substantial risk, especially to a newborn child. A non-invasive DNA test is increasingly being recommended instead.



Treatment

The standard therapy is a fructose-free diet. As long as patients with Hereditary Fructose Intolerance do not ingest fructose, they can lead normal lives. However, it is important that this disorder be diagnosed early, and the special diet adopted, to prevent permanent physical damage.

Investigational Therapies

Information on current clinical trials is posted on the Internet at www.clinicaltrials.gov. All studies receiving U.S. government funding, and some supported by private industry, are posted on this government web site.



For information about clinical trials being conducted at the NIH Clinical Center in Bethesda, MD, contact the NIH Patient Recruitment Office:



Tollfree: (800) 411-1222

TTY: (866) 411-1010

Email: prpl@cc.nih.gov



For information about clinical trials sponsored by private sources, contact:

www.centerwatch.com

References

TEXTBOOKS

Beers MH, Berkow R., eds. The Merck Manual, 17th ed. Whitehouse Station, NJ: Merck Research Laboratories; 1999:2389.



Bennett JC, Plum F., eds. Cecil Textbook of Medicine. 20th ed. Philadelphia, PA: W.B. Saunders Co; 1996:1083-85.



REVIEW ARTICLES

Ali M, et al., Hereditary fructose intolerance. J Med Genet. 1998;35:353-65.



Kerner JA Jr., Formula allergy and intolerance. Gastroenterol Clin North Am. 1995;24:1-25.



JOURNAL ARTICLES

Hillebrand G, et al., Hereditary fructose intolerance and alpha(1) antitrypsin deficiency. Arch Dis Child. 2000;83:72-73.



Lau J, et al., Screening for hereditary fructose intolerance mutations by reverse dot-blot. Mol Cell Probes. 1999;13:35-40.



Long WW, et al., Pathological case of the month. Hereditary fructose intolerance. Arch Pediatr Adolesc Med. 1997;151:1165-66.



James CL, et al., Neonatal screening for hereditary fructose intolerance: frequency of the most common mutant aldolase B allele (A149P) in the British population. J Med Genet. 1996;33:837-41.



Couper R., Hereditary fructose intolerance in an adult. Aust N Z J Med. 1996;26:231.



FROM THE INTERNET

McKusick VA., ed. Online Mendelian Inheritance in Man (OMIM). Baltimore. MD: The Johns Hopkins University; Entry No: 229600; Last Update: 2/4/2000.



HFI Laboratory at Boston University. Hereditary Fructose Intolerance. nd. 6pp.

www.bu.edu/aldolase/HFI



Brooks. DG. MEDLINEplus. Medical Encylopedia. Hereditary fructose intolerance11/12/01:3pp.

www.nlm.nih.gov/medlineplus/ency/article/000359.htm



Oxford Medicine Information. Fructose intolerance. 2/11/1996:2pp.

www.oxmedinfo.jr2.ox.ac.uk/Pathway/Disease/36355.htm



Hereditary fructose intolerance. 1999:2pp

www.hendrickhealth.org/healthy/00050990.html



HealthCentral. Hereditary fructose intolerance.

www.healthcentral.com/peds/top/000359.cfm



Duke University Medical Center. GSD Laboratory. Disorders of Fructose metabolism. 12/6/01:1p.

www.duke.edu/~mdfeezor/GSDHome/FructoseAssay.Html



Fructose Metabolism, Clinical Significances of Fructose Metabolism. 5/10/01:3pp.

www.indstate.edu/thcme/mwking/non-glucose-sugar-metabolism.html



Federal Drug Administration. FDA/ORA CPG 713. 5/22/87:1p.

www.fda.gov/ora/com[pliance_ref/cpg/cpgdrg/cpg400-335.html

Resources

NIH/National Institute of Diabetes, Digestive & Kidney Diseases

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Genetic and Rare Diseases (GARD) Information Center

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Internet: http://rarediseases.info.nih.gov/GARD/



For a Complete Report

This is an abstract of a report from the National Organization for Rare Disorders, Inc.® (NORD). Cigna members can access the complete report by logging into myCigna.com. For non-Cigna members, a copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html.

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