Keita, Aichata and Traoré, Bory and Dembélé, Adama and Diarra, Rokiatou and Diarra, Mariam and Cissé, Elmouloud M. and Kané, Mariam and Coulibaly, Bakary and Konaré, Hawa (2023) Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital. Open Journal of Pediatrics, 13 (06). pp. 831-837. ISSN 2160-8741
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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.
Item Type: | Article |
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Subjects: | R Medicine > RJ Pediatrics |
Depositing User: | Managing Editor |
Date Deposited: | 09 Nov 2023 11:00 |
Last Modified: | 09 Nov 2023 11:00 |
URI: | http://asian.go4publish.com/id/eprint/3217 |