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Mucopolysaccharide storage disease type VII

This type is also known as Goldberg syndrome β- Glucosidase deficiency. It is characterized by normal or slightly backward intelligence, bone changes, special face, dwarfism, hepatosplenomegaly and hernia. Excessive dermatan sulfate can be excreted in urine, which is an autosomal recessive disease. Although the biochemical defects are the same, the clinical manifestations and onset age of each case are different.

Symptoms

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

Pancreatic insufficiency with neutropenia syndrome in children

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