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.
General
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