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Mucopolysaccharidosis Type I
The most common type of mucopolysaccharidosis. It is inherited in an autosomal recessive pattern. It comprises a group of lysosomal storage diseases which includes the most severe form (Hurler syndrome) and the mildest form (Scheie syndrome). (NCI Thesaurus)
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The interface between the more apically located alveolar mucosa and the more coronally located gingiva.
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