Citations 1

Transient Neonatal Zinc Deficiency Due to a New Autosomal Dominant Mutation in Gene SLC 30A2 (ZnT‐2)

Pediatric Dermatology | January 23, 2014 | Volume: 31 | Issue: 2 | Pages: 251-252

10.1111/pde.12257 | PMID 24456035

Abstract Transient neonatal zinc deficiency ( TNZD ) has a clinical presentation similar to that of acrodermatitis enteropathica but is caused by a low zinc concentration in maternal breast milk. TNZD becomes clinically evident during breastfeeding and is resolved by weaning and the introduction of complementary nutrition. We present a 4‐month‐old girl with TNZD due to a new autosomal dominant mutation (663delC) in the maternal SLC 30A2 gene not previously described in the literature.