What else is it called?
- Catalase Deficiency
- Takahara Disease
Get in touch
Contact our caring team on 08452 412 173 for help and support. Our phone lines open 10am-4pm, Monday to Friday.
Prefer to email? Our email address is firstname.lastname@example.org.
What causes it?
Acatalasemia is caused by mutations (changes) in the CAT gene. This gene is responsible for giving instructions for making the enzyme catalase which breaks down hydrogen peroxide molecules into oxygen and water. Hydrogen peroxide is formed through chemical reactions within the cells. At low levels, it is used in chemical signalling pathways however, at high levels it is toxic to the cells. If hydrogen peroxide is not broken down by the enzyme catalase, it will be converted into compounds called reactive oxygen species that can damage DNA, proteins and cell membranes.
Mutations (changes) in the CAT gene greatly decreases the activity of the enzyme catalase. A lack of this enzyme can cause hydrogen peroxide to build up to toxic levels in certain cells. An example is a build-up of hydrogen peroxide produced by bacteria in the mouth can build up and damage soft tissues causing mouth ulcers and gangrene (a serious condition where a loss of blood supply causes body tissue to die). The build up of hydrogen peroxide also causes damage to beta cells of the pancreas which release insulin that controls blood sugar levels. This is why individuals with Acatalasemia are at risk to type 2 diabetes.
It is common for people to have reduced catalase activity with no identified mutation in the CAT gene. The cause of the condition in these cases is unknown.
How common is it?
More than 100 cases of this condition have been reported. It is estimated that the condition occurs in about 1 in 12,500 people in Japan, 1 in 20,000 people in Hungary and 1 in 25,000 people in Switzerland. The prevalence of this condition in other populations in unknown.
What are the signs and symptoms?
Many individuals with this condition show no symptoms and never have any related health problems. The only reason they are diagnosed is because they have affected family members.
Some of the first patients that were reported with Acatalasemia had:
- Ulcers (open sores) inside the mouth
- Gangrene (the death of soft tissue) in the mouth
The condition is known as Takahara disease when Acatalasemia occurs with mouth ulcers and gangrene. This is rarely seen in more recent cases, most likely due to improved oral hygiene.
Individuals with Acatalasemia also have an increased risk of developing type 2 diabetes.
How is it diagnosed?
A diagnosis usually starts with a full medical history, investigation of symptoms and a physical examination. Molecular genetic testing can confirm the diagnosis by showing mutations (changes) in the CAT gene.
Can it be treated?
There is currently no cure for Acatalasemia. With the main symptoms being related to oral ulcers and gangrene, periodontal (gum disease) treatments are used to reduce tissue damage and improve oral hygiene.
Do my family need to be tested?
Acatalasemia is an inherited condition. Humans have chromosomes made up of DNA. Genes are pieces of DNA that carry the genetic information. Each chromosome may have several thousand genes. We inherit chromosomes from the egg of the mother and sperm of the father. The genes on those chromosomes carry the instructions that determine a person’s characteristics, which are a combination of the parents.
The pattern of inheritance of Acatalasemia is autosomal recessive. This means that carriers of the condition do not have the disorder because the other gene of this pair is working normally. Parents of children with Acatalasemia are carriers.
When both parents are carriers, the risk to the baby in each pregnancy is:
- There is a 50% chance that the child will inherit one faulty and one working gene, which means they will also be a carrier.
- There is a 25% chance that the child will inherit two working genes and not inherit or carry the faulty gene.
- There is a 25% chance that the child will inherit two faulty genes, which means they will have Biotinidase Deficiency.
If you think you, or somebody in your family, may have Biotinidase Deficiency, or that you may be a carrier, contact your medical team who may refer you for genetic testing.
References are available on request. Please contact Helen Morris by phoning 0845 241 2173 or emailing email@example.com [Resource Library No: AAP002].