Примери коришћења Glycogen storage на Енглеском и њихови преводи на Српски
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Glycogen storage disorders are rare.
What is the outlook for glycogen storage disorders?
Glycogen storage disorders are inherited.
Someone can be a carrier for a glycogen storage disorder.
Glycogen storage diseases(types 1 and 3).
The different types of glycogen storage disorder include.
Glycogen Storage Disorders are extremely rare.
In fact, there are over 12 types of glycogen storage disorder.
Who gets glycogen storage disorders?
This can help to confirm the type of glycogen storage disorder.
Glycogen storage diseases: New perspectives.
Errors in this gene cause glycogen storage disease type II(Pompe disease).
Glycogen storage disorders are a group of inherited diseases.
The outlook(prognosis) depends on the type of glycogen storage disorder that you have.
Glycogen storage disorders are hereditary conditions that run in families.
A high-protein diet may also be helpful in some glycogen storage disorders.
Most people with a glycogen storage disorder respond well to treatment.
Your doctor will be able to discuss the outlook for a particular glycogen storage disorder in more detail.
Most, but not all, glycogen storage disorders are inherited in a pattern called autosomal recessive inheritance.
It is estimated that about one baby in every 20,000 to 40,000 babies born has a glycogen storage disorder.
This is because certain types of glycogen storage disorders can cause heart problems.
The geneticist will be able to discuss the likelihood of your future child, or children,having a glycogen storage disorder.
If your doctor suspects that you oryour child may have a glycogen storage disease, they may suggest the following investigations.
Some glycogen storage disorders, particularly type Ib, can affect your immune system and make you more susceptible to infections.
Other tests are sometimes carried out depending on the type of glycogen storage disorder that your doctor suspects.
However, type II glycogen storage disorder(infantile Pompe's disease) can be difficult to treat and can affect life expectancy.
Enzyme replacement therapy andgene therapy mean that it is hoped that the outlook for glycogen storage disorders will soon be greatly improved.
Some people with glycogen storage disorders who do not respond to nutritional supplements may occasionally need a liver transplant.
Because there are a number of different enzymes involved in glycogen production andbreakdown, there are a number of different glycogen storage disorders.
People with glycogen storage disorders affecting their immune system may need to take regular antibiotic medication to protect against infection.