Zinc deficiency in infants: a rare case of enteropathic acrodermatitis?

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Bruna K. Pinheiro França Protásio
Mauro Sérgio Toporovski
Lygia Souza Lima Lauand
Clarice Blaj Neufeld
Leandro Dimasi Buck
Laura Garofalo
Luciana de Almeida
Camila M. P. Machado Martins Barbosa

Abstract

Introduction: enteropathic acrodermatitis is a rare hereditary disorder of zinc metabo­lism, and may present with malnutrition, diarrhea, alopecia, dermatitis and recurrent infec­tions. The certainty diagnosis is made by the genetic test. Objective: to report a case of zinc deficiency in infants with a typical clinical picture of enteropathic acrodermatitis, whi­ch, although suggestive, could not be confirmed by genetic testing. Case description: an 11 month old patient with dermatitis, chronic diarrhea and zinc deficiency started after weaning from breast milk with initial improvement after zinc replacement and death due to sepsis. Discussion: in this case report, we have a patient attended in a hospital whe­re the specific test isn’t available, however the clinical, laboratory and evolution are quite suggestive of this disease. The treatment is the zinc replacement and it’s results is satisfactory.

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Bruna K. Pinheiro França Protásio, Mauro Sérgio Toporovski, Lygia Souza Lima Lauand, Clarice Blaj Neufeld, Leandro Dimasi Buck, Laura Garofalo, … Camila M. P. Machado Martins Barbosa. (2017). Zinc deficiency in infants: a rare case of enteropathic acrodermatitis?. Revista De Pediatria SOPERJ, 17(3), 34–37. Retrieved from https://revistadepediatriasoperj.org.br/rps/article/view/331
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