What is hereditary fructose intolerance (HFI)?
We get asked this question a lot – so I though I would write a special
post for you all…
HFI is an inherited (genetic) condition where a person is born unable to
digest the sugar fructose. Unlike
fructose malabsorption, where symptoms occur because the cells of the bowel
cannot absorb fructose; HFI is a deficiency and inability to produce the liver
enzyme (fructose 1-aldolase, to be
technical!) needed to breakdown fructose. Symptoms of HFI are only seen when the
child eats fructose for the first time and if left untreated can cause severe
health problems for the child.
How common is HFI?
About 1 in every 25,000 people are reported to have HFI
How common is Fructose
malabsorption?
About 1 in 3 people have fructose malabsorption.
Treatment of HFI
Elimination of fructose, sucrose and sorbitol under the guidance of
Paediatrician and dietitian.
This differs from fructose malabsorption, where small to moderate
amounts of fructose can still be consumed without symptoms when balanced out
with a higher proportion of glucose.
There are often lots of terms thrown around these days and some
incorrectly used interchangeably. In this case, I hope this clarifies the
difference between HFI and fructose malabsorption for you.
G xx
By Georgie Rist. Accredited Practising Dietitian (APD), Accredited Nutritionist, and Sports Dietitian
By Georgie Rist. Accredited Practising Dietitian (APD), Accredited Nutritionist, and Sports Dietitian
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