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Hunter's syndrome

   Also found in: Wikipedia 0.07 sec.
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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His dwarfed body was wasted as was his mind by Hunter's syndrome, and he was near death, but I handled him with all the reverence with which I used to handle the sacraments when I was a priest.
 
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