Acrodermatitis enteropathica (AE) is a rare zinc deficiency–related dermatosis in children, often resembling other dermatologic disorders and posing a diagnostic challenge. Due to its rarity and non-specific presentation, AE is frequently underrecognized at initial evaluation, leading to suboptimal treatment responses and potentially serious complications. We report a successfully treated case of AE, emphasizing that zinc deficiency should be considered in infants with persistent dermatitis unresponsive to standard treatments, in order to improve outcomes and reduce misdiagnosis.
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Ngo et al. (2026) studied this question.
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