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Pediatr Dermatol ; 31(2): 251-2, 2014.
Article in English | MEDLINE | ID: mdl-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 SLC30A2 gene not previously described in the literature.


Subject(s)
Cation Transport Proteins/genetics , Metal Metabolism, Inborn Errors/genetics , Mutation , Female , Growth Disorders , Humans , Infant , Metal Metabolism, Inborn Errors/drug therapy , Milk, Human/chemistry , Zinc/therapeutic use
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