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Lactose Intolerance History

Lactose intolerance is a worldwide phenomenon that has been widely studied over the years in order to understand the influences of human evolution and migration over the ages.

7 Jun 2010

Among people with lactose intolerance, the consumption of milk and dairy products may lead to several symptoms including abdominal discomfort, diarrhea and flatulence. Lactose intolerant individuals therefore tend to avoid consuming milk and milk products.

7 Jun 2010

Managing Lactose Intolerance

Lactose intolerance is treated depending on how extreme the sensitivity to lactose in food is. In most individuals, monitoring the diet and avoiding foods with lactose helps to prevent the symptoms of lactose intolerance.

7 Jun 2010

Lactase Biology

Lactase is an enzyme present in the gut that is responsible for breaking down complex lactose sugars into simpler sugars such as glucose and galactose which can then be utilized for energy and bodily functions.

7 Jun 2010

Lactose Intolerance Diagnosis

Lactose intolerance is frequently and mistakenly self-diagnosed. In babies, it is also often confused with cow milk allergy. Diagnosis should not be based on clinical symptoms alone and should be made by a physician who has performed certain laboratory tests.

7 Jun 2010

What is Lactose Intolerance?

Lactose intolerance describes a condition where a person is incapable of digesting lactose - a type of sugar present in milk and dairy products. Food intolerance is different from food allergy. While symptoms of allergy may be brought about by consuming even tiny amounts of a certain food, the amount that brings about the symptoms of intolerance varies from person to person.

7 Jun 2010

Fabry Disease Diagnosis

Fabry disease is an X-linked recessive disorder that leads to the accumulation of a lipid called globotriaosylceramide in the cells of the body. The condition is rare and affects around 1 in 50,000 males. As an X-linked condition, Fabry disease mainly affects males, although females can also be affected.

7 Jun 2010

Fabry Disease Treatments

Fabry disease is a genetic lysosomal storage disease that progresses with age and cannot be cured. The disease is caused by a deficiency in the enzyme α-galactosidase A, which leads to a build up in cells of a glycolipid called globotriaosylceramide (also called ceramide trihexoside or Gb3 or GL-3). This glycolipid gets deposited in the blood vessels, tissues and organs, eventually disrupting their function.

7 Jun 2010

Fabry Disease Symptoms

Fabry disease is an X-linked recessive disorder, meaning the condition is caused by a gene defect present on the X chromosome. Males who inherit the gene defect on their single X chromosome experience a more severe form of the disease compared with females, who may also inherit a normal X chromosome.

7 Jun 2010

What is Fabry Disease?

Fabry disease is a rare genetic condition that belongs to a group of disorders referred to as lysosomal storage disease.

7 Jun 2010

Galactosemia Treatments

Galactosemia is an inherited genetic disorder of metabolism where the body is unable to metabolize a sugar called galactose.

7 Jun 2010

Galactosemia Causes

Galactosemia is a rare genetic disorder where galactose (a by-product of lactose digestion) fails to convert to glucose.

7 Jun 2010

Galactosemia Diagnosis

Galactosemia is a rare genetic disorder in which galactose cannot be converted to glucose and instead accumulates in the blood. If infants born with this condition are left untreated, they die in 75% of cases.

7 Jun 2010

What is Galactosemia?

Galactosemia is a rare genetic disorder that causes an inability to digest galactose, which is a breakdown product of lactose.

7 Jun 2010

How is Acromegaly Treated?

Treatment of Acromegaly aims to reduce excess growth hormone, relieve the pressure that the tumour is exerting on the surrounding structures and thus improve symptoms of the disease. If not treated the condition may worsen and eventually lead to severe symptoms and death.

7 Jun 2010