less than 30 years
Morquio syndrome is an inherited disease of metabolism in which the body is missing or doesn't have enough of a substance needed to break down long chains of sugar molecules called glycosaminoglycans
20-60 years if its the mild type, and 10-20 years if its the more severe type.
The treatment may last about six months, but in some cases may last as long as a year.
Kevin had a birth defect called Morquio Syndrome. Morquio Syndrome is an inherited disease in which a person does not have enough of a substance called glycosaminoglycans. Glycosaminoglycans break down long chains of sugar molecules, called keratan sulfate. The syndrome belongs in a bigger group called mucopolysaccharidoses, also known as MPS IV. One type of Morquio Syndrome is Type A, which means the person lacks the enzyme galactosamine 6 sulfatase. The other type, Type B, means the enzyme beta- galactosidase is lacking. If the body lacks either of these enzymes, it can not break down the glycosaminoglycan, so it builds up in the body and brain, which can damage organs. The syndrome occurs in one of every 200,000 births. The only way a child can get Morquio is if both parents either have it, or are carriers because it is a autosomal recessive trait.
two weeks
Morquio syndrome is an autosomal recessive trait. That means both your parents must pass you the defective gene in order for you to get this disease.There are two forms of Morquio syndrome: Type A and Type B.Persons with Type A do not have a substance (enzyme) called galactosamine-6-sulfatase.Persons with Type B do not produce enough of an enzyme called beta-galactosidase.The body needs these enzymes to break down a long strand of sugar molecules called the keratan sulfate sugar chain. In both types, abnormally large amounts of glycosaminoglycans build up in the body and brain, which can damage organs.The syndrome is estimated to occur in 1 of every 200,000 births. Symptoms usually start between ages 1 and 3. A family history of the syndrome raises one's risk for the condition.
depend on treatment it can last up to one weak
Stickler syndrome is a genetic disorder that is present from birth and persists throughout a person's life. The symptoms and severity of the condition can vary widely among individuals, but the genetic mutation that causes Stickler syndrome is lifelong. Treatment is focused on managing symptoms and complications associated with the syndrome.
5 to 14 days
It depends on how much treatment you have
Serotonin syndrome can resolve within 24 hours if the offending medications are discontinued, but the duration can vary based on the severity of symptoms and individual factors. Without treatment, some symptoms may persist longer, particularly if there are underlying health issues or if multiple serotonergic drugs are involved. Long-term effects are generally rare, but in severe cases, prolonged serotonin syndrome can lead to complications such as seizures, muscle damage, or changes in mental status. Prompt recognition and treatment are essential to avoid these potential long-term consequences.