Test Details: Deficiency of the alpha-L-Iduronidase causes development of Mucopolysaccharidosis Type I. There is lysosomal accumulation of glycosaminoglycans leading to progressive cellular and multiorgan dysfunction. Symptoms include skeletal deformities, delayed motor and intellectual development, corneal clouding, organomegaly, heart disease, short stature, hernia, facial dysmorphism.
Advanced Routine Diagnostics
Sample should reach to lab within 12 to 24 Hrs.
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