Examples of 'hunter syndrome' in a sentence
Meaning of "hunter syndrome"
hunter syndrome - Hunter syndrome, also known as mucopolysaccharidosis type II (MPS II), is a genetic disorder that primarily affects males. It is characterized by a deficiency or absence of the enzyme iduronate 2-sulfatase, which leads to the accumulation of certain complex carbohydrates in the body, causing a wide range of physical and neurological symptoms.
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- A lysosomal storage disease caused by a deficient (or absent) enzyme, iduronate-2-sulfatase.
How to use "hunter syndrome" in a sentence
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hunter syndrome
Hunter syndrome may present with a wide variety of phenotypes.
Elaprase is used to treat patients with Hunter syndrome.
Hunter syndrome is genetic problem in which malfunctioning of enzyme occurs in the body.
This is the best method to prevent Hunter syndrome.
Hunter syndrome occurs mostly in boys and affects many different parts of the body.
This medicine is used for the treatment of Hunter syndrome.
Patients with Hunter syndrome have insufficient levels of this enzyme.
There is a broad range of severity in the symptoms of Hunter syndrome.
The first sign of Hunter Syndrome is a visible change in facial features of the baby.
Molecular and phenotypic variation in patients with severe Hunter syndrome.
Hunter syndrome is one of several related lysosomal storage diseases called the MPS diseases.
Two relatively distinct clinical forms of Hunter syndrome have been recognized.
Idursulfase replaces the enzyme that is missing or defective in patients with Hunter syndrome.
Hurler syndrome and Hunter syndrome are members of the same group of inherited metabolic disorders.
You can be a part of a registry for patients with Hunter syndrome.
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The sleep patterns of a child with Hunter syndrome can become more and more disorganized.
It replaces the enzyme that is missing or defective in patients with Hunter syndrome.
Physical manifestations for some people with Hunter syndrome include distinct facial features and large head.
A medical example is a heterokaryon composed of nuclei from Hurler syndrome and Hunter syndrome.
Learn more about Hunter syndrome.
An experienced anesthesia specialist should perform the intubation of a person with Hunter syndrome.
Hunter Syndrome has no cure.
This is by far the best way to prevent Hunter Syndrome.
Hunter syndrome is a rare hereditary condition characterized by malfunction or absence of enzyme iduronate 2-sulfatase.
Multidisciplinary management of Hunter syndrome.
Since Hunter syndrome is an X-linked recessive disorder, it preferentially affects male patients.
Madeux has a metabolic disease called Hunter Syndrome.
Hunter Syndrome Symptoms HunterSyndrome . info.
Certain embodiments therefore include the treatment of Hunter Syndrome with CNS involvement.
Hunter syndrome is almost always severe, progressive and life-limiting.
A physical exam and tests in someone with Hunter syndrome may show,.
However, Hunter syndrome is always progressive and life-limiting.
In particular embodiments, the subject has a lysosomal storage disorder, such as Hunter Syndrome.
Generally, physical manifestations for people with Hunter syndrome include both somatic and neuronal symptoms.
The invention also provides a composition of the invention, for use in treating Hunter syndrome.
Patients with Hunter syndrome do not produce an enzyme called iduronate-2-sulfatase.
However, there are some treatments that are coming up for Hunter Syndrome.
Hunter syndrome is an X-linked disease caused by insufficient levels of the lysosomal enzyme iduronate-2-sulfatase.
ELAPRASE is a long-term enzyme replacement therapy in patients with Hunter syndrome.
Patients with Hunter syndrome do not produce enough of their own enzyme, iduronate-2-sulfatase.
Lysosomal storage diseases having a CNS etiology or component, includes Hunter syndrome.
The symptoms of Hunter syndrome ( MPS II ) are generally not apparent at birth.
Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II Hunter syndrome.
Hunter syndrome is also called mucopolysaccharidosis II ( MPS II ).
Sign up for new information about Hunter syndrome ( MPS II ).
As a result, Hunter syndrome is always severe, progressive, and life-limiting.
In certain embodiments, the lysosomal storage disease is Hunter Syndrome ( MPS II ).
What is hunter syndrome ( MPS II ).
Mutations of the iduronate-2-sulfatase ( IDS ) gene in patients with Hunter syndrome mucopolysaccharidosis II.
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