Mucopolysaccharidosis type VI, also known as Maroteaux-Lamy syndrome or polydystrophic dwarfism, is an autosomal recessive genetic disease. It is characterized by short stature and corneal opacity, but normal intelligence. This type of mucopolysaccharidosis was first discovered by Maroteaux (1963) and is an independent disease different from other types of mucopolysaccharidosis.
This section is being translated and completed.
This section is being translated and completed.
This section is being translated and completed.
This section is being translated and completed.
This section is being translated and completed.
This section is being translated and completed.
This section is being translated and completed.
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This information is for health education only and is not a diagnosis. Please consult a qualified clinician if you feel unwell.