THE complication of vitamin A deficiency was noted in early descriptions of cystic fibrosis as a clinical entity.1,2 Treatment aimed at improving intestinal absorption in this disease and availability of water miscible vitamin A have made clinically evident vitamin A deficiency rare. This report describes an adolescent girl with cystic fibrosis who exhibited xerophthalmia and night blindness when first seen. Light and electron microscopic examination of the conjunctiva as well as serial dark adaptation studies and vitamin A determinations are presented to document the deficiency and its response to pancreatic extract (Viokase) therapy.
Report of a Case
This 16-year-old girl (CH No. 377211) was referred to the Nutrition Clinic in September 1966 by a social agency. She had been seen in our outpatient department between 10 and 15 months of age for what was thought to be allergic diarrhea, and then was lost to follow-up. At 10 years
Petersen RA, Petersen VS, Robb RM. Vitamin A Deficiency With Xerophthalmia and Night Blindness in Cystic Fibrosis. Am J Dis Child. 1968;116(6):662–665. doi:10.1001/archpedi.1968.02100020666016
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