I-Cell Disease: Causes and Treatment Options

By John Smith
Published by Andale LLC
$9.99 Rating: Not yet rated.
Published: Oct. 31, 2011
Words: 15,730 (approximate)
Language: English
ISBN: 9781466166097


Short description

I-cell disease, or Inclusion-cell disease, is an extremely rare inherited metabolic disorder characterized by coarse facial features, skeletal afflictions and developmental delays. If this disorder has touched your life, this book gives you the information you need to know about causes and treatment options.

Extended description

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.

Tags

leroy disease, inclusion cell disease, gnpta, icell disease

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