20-60 years if its the mild type, and 10-20 years if its the more severe type.
less than 30 years
people (girls/women) with turner syndrome live as long as regular people do....turner syndrome does not affect life spancy
people with ushers syndrome will have a normal life expectancy
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
people can live up to 60 to 70 years.
They live normal, long, healthy lives. The syndrome has been in my family for generations, and many live 85 years ore longer.
People with Angelman Syndrome usually have a normal life span unless they have it severe or a bad rare kind of it. This can be followed up by looking for the symptoms.
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.
16 years
50 to 60 years of age
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.
There's no shortening of life expectancy. The condition is manageable throughout the sufferers life.