Acrodermatitis Enteropathica: Case Report Analyses of Zinc Metabolism, Electron Microscopic Examination, and Immune Function

    Sevgi Gözdaşoğlu, Nurdan Taçyıldız, Ayla Günlemez, Hi̇kmet Bayhan, Huriye Sencer, Emel Ünal, Aydan İkincioğulları, H. İnceoğlu, Serap Aksoylar, G. Yavuz, Mehmet Ertem
    Studysummary In this case report, an 11-year-old girl with acrodermatitis enteropathica experienced a complete resolution of symptoms following oral zinc therapy, highlighting its effectiveness in managing this condition.
    Our plain-language summary. Not medical advice or a treatment recommendation. Consult a qualified healthcare professional before changing treatment. Full disclaimer
    This case report detailed an 11-year-old girl with acrodermatitis enteropathica (AE), a rare autosomal recessive disorder affecting zinc metabolism, which manifested with rashes, growth retardation, partial alopecia, and other symptoms. Laboratory tests showed decreased zinc levels in various body compartments despite normal absorption, and electron microscopy revealed Paneth cell inclusions in the intestinal mucosa. Abnormalities were also noted in lymphocyte subpopulations and neutrophil chemotaxis. The patient's symptoms resolved completely within weeks following oral zinc therapy.
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