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Hunter syndrome, or mucopolysaccharidosis type II (MPS II), is a rare genetic disorder in which large sugar molecules called glycosaminoglycans (or GAGs or mucopolysaccharides) build up in body tissues.
Jul 27, 2023 · Hunter syndrome is a rare genetic disorder that affects physical and mental development. Learn about the signs, diagnosis, management and outlook of this condition from Cleveland Clinic experts.
May 1, 2024 · Hunter syndrome is a rare genetic disorder that affects mostly males and causes the buildup of sugar molecules in the body. Learn about the symptoms, causes, diagnosis, treatment, and outlook of this condition.
Jul 25, 2023 · Mucopolysaccharidosis Type II (Hunter syndrome) is a rare X-linked recessive disorder. It has an early age of onset with clinical symptoms involving multiple organ systems. The severity of the disease depends on the phenotype. The severe phenotype has high morbidity and mortality.
Hunter syndrome is a genetic condition that affects boys and causes short stature, joint problems, hearing loss and more. Learn about the symptoms, causes and diagnosis of this rare disorder from Mass General for Children.
Hunter syndrome is a progressive disorder that affects many organs and tissues, especially in boys. It has two types: neuropathic and non-neuropathic, with different rates of progression and life expectancy.
MPS II is a rare, inherited disorder that affects boys and causes an abnormal accumulation of complex sugars in cells. Learn about the symptoms, causes, diagnosis and treatments of this condition from the Lysosomal Storage Disorders Program at Boston Children's.
