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Mucopolysaccharide storage disease type VI

This type is also known as Maroteaux Lamy syndrome and multiple dystrophic dwarfism. It is also an autosomal recessive disease. It is characterized by short stature, cloudy cornea, but normal intelligence. This type of mucopolysaccharide storage disease was first discovered by Maroteaux (1963). It is an independent disease different from other types of mucopolysaccharide storage disease.

Symptoms

Mucopolysaccharide storage disease type VII

Mucopolysaccharidosis type VIII

mitral stenosis

Mitral insufficiency

Childhood leukemia

Malignant histiocytosis

Otogenic brain abscess

Combined diseases of mitral valve, aortic valve and tricuspid valve

Malignant pleural effusion

Mitral insufficiency

Diseases of mitral and aortic valves

Carbon disulfide poisoning

Calcification of mitral annulus

Nitrogen dioxide poisoning

Mitral valve prolapse syndrome

Malignant hypertension

Malignant atrophic papulosis

Second degree atrioventricular block

Nausea and vomiting

Abdominal pain in children

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