Clinical Features and Genetic Analysis of Acrodermatitis Enteropathica in an Ethnic Minority Infant from Western China: A Case Report and Literature Review

    Tuerhongjiang Axirejiang (22346272), Gulinigeer Simayi (22346275), Abudushalamu Abuduwake (22346278), Yunxia Liu (414102), Gang Zheng (29050), Irshat Ibrahim (10855258)
    Studysummary In this case study, a 10-month-old minority infant from Xinjiang, China, with acrodermatitis enteropathy caused by an SLC39A4 gene mutation showed clinical improvement and increased zinc levels following zinc supplementation, highlighting the importance of early genetic testing and customized treatment in managing the disorder.
    Our plain-language summary. Not medical advice or a treatment recommendation. Consult a qualified healthcare professional before changing treatment. Full disclaimer
    Discuss this study in the Community โ†’