Literature DB >> 7377790

Hereditary acrodermatitis enteropathica in an adult.

K Graves, T Kestenbaum, J Kalivas.   

Abstract

The condition of a 33-year-old woman who had a history of blisters following trauma on the hands, knees, and feet since 1 year of age previously had been diagnosed as epidermolysis bullosa. She also had psoriasiform plaques, a pustular crusted periorificial eruption, paronychia, alopecia, and photophobia. She had had minimal history of diarrhea. A markedly decreased serum zinc level was found, and treatment with zinc sulfate was instituted, resulting in clearing of all clinical manifestations. Since patients with hereditary acrodermatitis enteropathica may have minimal or no diarrhea and the correct diagnosis may be long delayed, the condition should not be considered strictly a disease of children.

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Year:  1980        PMID: 7377790

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN: 0003-987X


  4 in total

1.  Acrodermatitis enteropathica.

Authors:  P J Aggett
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

2.  Zinc deficiency and its inherited disorders -a review.

Authors:  M Leigh Ackland; Agnes Michalczyk
Journal:  Genes Nutr       Date:  2006-03       Impact factor: 5.523

Review 3.  Clinical and laboratory diagnosis of acrodermatitis enteropathica.

Authors:  J P Van Wouwe
Journal:  Eur J Pediatr       Date:  1989-10       Impact factor: 3.183

4.  Acrodermatitis enteropathica.

Authors:  P S Mortimer; P Gough; P C Newbold; R P Dawber; T J Ryan
Journal:  J R Soc Med       Date:  1984-01       Impact factor: 18.000

  4 in total

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