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Novel SLC39A4 Mutation in Acrodermatitis Enteropathica

Authors


Address correspondence to Wendy Chung, M.D., Ph.D., Herbert Irving Assistant Professor of Pediatrics and Medicine, Director of Clinical Genetics, Columbia University, 1150 St. Nicholas Avenue, Room 620, New York, NY 10032, or e-mail: wkc15@columbia.edu.

Abstract

Abstract:  Acrodermatitis enteropathica (AE) is a rare autosomal-recessive disorder characterized by dermatitis, alopecia, diarrhea, and retardation of growth and development. AE maps to 8q24.3 and is associated with mutations in the intestinal zinc transporter ZIP4 encoded by the gene SLC39A4. We describe a novel homozygous mutation, 1191insC, in SLC39A4 in a patient from Sierra Leone and suggest that AE should be considered within the differential diagnosis for acrodermatitis in children from Sierra Leone. Genetic testing for this founder mutation can be easily performed for this treatable disorder.

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