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 Hunter Syndrome It interferes with the body' s ability to break down and recycle specific mucopolysaccharides, also known as glycosaminoglycans or GAG. Hunter
Наименование:

Hunter Syndrome

автор Frederic P. издательство Книга по Требованию Ветеринарный справочник традиционных и нетрадиционных методов лечения
Cтраниц 64        мягкая обложка       
Аннотация:It interferes with the body' s ability to break down and recycle specific mucopolysaccharides, also known as glycosaminoglycans or GAG. Hunter syndrome is one of several related lysosomal storage diseases. In Hunter syndrome, GAG builds up in cells throughout the body due to a deficiency or absence of the enzyme iduronate-2-sulfatase. This buildup interferes with the way certain cells and organs in the body function and leads to a number of serious symptoms. As the buildup of GAG continues throughout the cells of the body, signs of Hunter syndrome become more visible. Physical manifestations for some people with Hunter syndrome include distinct facial features and large head. Hunter syndrome, or mucopolysaccharidosis Type II, is a lysosomal storage disease caused by a deficient enzyme, iduronate-2-sulfatase . Born in Scotland, Hunter emigrated to Canada and had a medical practice in Winnipeg, Manitoba. Hunter syndrome, or mucopolysaccharidosis II, is a serious genetic disorder that primarily affects males. High Quality Content by WIKIPEDIA articles! The syndrome is named after physician Charles A. Hunter, who first described it in 1917.
Автор: Frederic P.
Издательство: Книга по Требованию
Год:2010
Цена:
1190 руб
Нет в наличии
Поиск: Hunter Syndrome
НОВЫЙ ГОД СИМВОЛ 2013 ГОДАУКРАШЕНИЯ
КАРНАВАЛ НА НОВЫЙ ГОД РАСПРОДАЖА
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