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Hunter's syndrome

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Hunter's syndrome
n.
A metabolic deficiency syndrome caused by a lack of certain sulfatase and by an inability to break down mucopolysaccharides and characterized by the presence of mucopolysaccharides in connective tissue. Also called type II mucopolysaccharidosis.
Hunter's syndrome
Etymology: Charles Hunter, Canadian physician, 1873-1955; Gk, syn, together, dromos, course
a hereditary defect in mucopolysaccharide metabolism affecting only males, characterized by dwarfism, kyphosis, gargoylism, and mental retardation. It is transmitted as an X-linked recessive trait. Females who carry the gene can be identified by biochemical tests. Also called MPS II, X-linked mucopolysaccharidosis. See also mucopolysaccharidosis.


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Hunter's Syndrome causes cells in the body to be constantly damaged to the point where the body becomes completely crippled.
It's a dream come true. I have been a fan of the Walker Brothers ... by Evening Chronicle (Newcastle, England)
Mary Wragg, 41, said her ex-husband told friends, his parents and a very ill girl's mum he would end the life of Jacob, 10, if the condition slowly killing him, Hunter's Syndrome, worsened.
'EX VOWED TO KILL SON' by The Mirror (London, England)
Andrew Wragg, of Worthing, West Sussex, appeared at Chichester Magistrates' Court charged with murdering his 10-year-old son Jacob, who suffered from Hunter's Syndrome.
Dad held over son's death by Daily Post (Liverpool, England)
 
 
 
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