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A novel SLC39A4 gene mutation in the family of an acrodermatitis enteropathica patient with an unusual presentation

✍ Scribed by S. Wang; L. Xue; Z-P. Guo; L. Wang; Y. Yang


Book ID
108670240
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
165 KB
Volume
159
Category
Article
ISSN
0007-0963

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Acrodermatitis enteropathica (AE) is a very rare inherited recessive disease caused by severe zinc deficiency. It typically occurs in early infancy and is characterized by periorificial and acral dermatitis, alopecia, and diarrhea. In 2002, both we and others identified the AE SLC39A4 gene located a