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Up to: Lysosomal storage disease with skeletal involvement · Familial mucolipidosis · GNPTAB-mucolipidosis
Mucolipidosis type III, alpha/beta
Mucolipidosis III alpha/beta (MLIII alpha/beta) is a lysosomal disorder characterized by progressive slowing of the growth rate from early childhood, stiffness and pain in joints, gradual coarsening of facial features, moderate developmental delay and mild intellectual disability in most patients.
This condition has no sub-types.