Perafan-Riveros, C., Franca, L.F., Alves, A.C. and Sanches Jr., J.A. (2002) Acrodermatitis Enteropathica: Case Report and Review of the Literature. Paediatrics Dermatology, 19, 426-431.
https://doi.org/10.1046/j.1525-1470.2002.00200.x

has been cited by the following article:

• TITLE: Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital

  AUTHORS: Aichata Keita, Bory Traoré, Adama Dembélé, Rokiatou Diarra, Mariam Diarra, Elmouloud M. Cissé, Mariam Kané, Bakary Coulibaly, Hawa Konaré

  KEYWORDS: Enteropathica Acrodermatitis, Necrotizing Fasciitis, Infant

  JOURNAL NAME: Open Journal of Pediatrics, Vol.13 No.6, November 8, 2023

  ABSTRACT: Acrodermatitis enteropathica is a rare autosomal recessive genetic disorder characterised by periorificial dermatitis, alopecia and diarrhoea. It is caused by a mutation in the gene that codes for a membrane protein that binds zinc. We report a case in a 7-month-old girl, admitted with altered general condition and scaly, pustular erythematous lesions, initially located in the occipital and cervical regions, and secondarily inguinal and on the knees. Management and outcome in this patient? Genetic assay was not available to confirm this rare genetic disease. A delay in establishing the diagnosis and a disastrous outcome did not save the patient despite the administration of zinc.