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Article
June 1970

Peripheral Corneal Opacification and Skeletal DeformitiesA Newly Recognized Acid Mucopolysaccharidosis Simulating Rheumatoid Arthritis

Author Affiliations

New York; Boston
From the Department of Ophthalmology, New York Hospital-Cornell Medical Center, New York (Dr. Brown), and the Massachusetts Eye and Ear Infirmary, Boston (Dr. Kuwabara).

Arch Ophthalmol. 1970;83(6):667-677. doi:10.1001/archopht.1970.00990030667001
Abstract

Two female siblings, ages 5 and 13, had conditions diagnosed as mucopolysaccharidosis by the presence of increased mucopolysaccharides of the skin culture of the sisters and both parents. In addition to many signs common to the mucopolysaccharidoses, they had severe progressive intraarticular joint destruction and peculiar progressive peripheral annular corneal opacifications. The latter signs indicate that these sisters represent a new mucopolysaccharidosis.

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