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November 02 , 2009

I-Cell Disease: Causes and Treatment Options


I-cell disease, or Inclusion-cell disease, is an extremely rare inherited metabolic disorder characterized by coarse facial features, skeletal afflictions and developmental delays. I-cell disease is also known as: GNPTA, Inclusion Cell Disease, Leroy Disease, ML Disorder, Type II, ML II, Mucolipidosis II, or N-Acetylglucosamine-1-Phosphotransferase Deficiency. If this disorder has touched your life, this book gives you the information you need to know about causes and treatment options.

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In 1970, after serving nearly twenty years in Nigeria, John Smith returned to the Foreign and Commonwealth Office ready for a fresh assignment as a Commonwealth administrator. The ‘powers that be’ assured him that they would find him ‘an island in the autumn’ The posting turned out to be that of Financial Secretary of the Solomon islands, where he…

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