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Published on: September 20, 2018
Acquired Zinc Deficiency Mimicking Acrodermatitis Enteropathica in a Breast-Fed Premature Infant
Giovanna D'Amico1, Corinne De Laet2, Guillaume Smits3,4,5
1Department of Pediatrics, Hôpital Universitaire des Enfants Reine Fabiola, Université Libre de Bruxelles, Avenue Jean Joseph Crocq 15, 1020 Brussels, Belgium.
Insights
Transient acquired zinc deficiency can affect premature infants, presenting with skin issues similar to acrodermatitis enteropathica. Prompt zinc supplementation is crucial for recovery in these cases.
Area of Science:
- Pediatrics
- Dermatology
- Nutritional Science
Background:
- Premature infants have increased nutritional requirements, making them susceptible to deficiencies.
- Acquired zinc deficiency can manifest with dermatological symptoms resembling genetic conditions.
- Maternal factors, such as low serum and milk zinc levels, can impact infant nutrition.
Observation:
- A 4-month-old premature male infant presented with an acrodermatitis enteropathica-like rash.
- Laboratory tests revealed low zinc levels in the infant, mother's serum, and breast milk.
- Genetic testing excluded mutations in the SLC39A4 gene, ruling out hereditary acrodermatitis enteropathica.
Findings:
- The infant's condition was diagnosed as transient acquired zinc deficiency.
- Low maternal zinc levels and breast milk zinc content were identified as contributing factors.
- The absence of genetic mutations indicated an acquired, rather than inherited, condition.
Implications:
- This case highlights the importance of monitoring zinc levels in premature infants and breastfeeding mothers.
- Early diagnosis and zinc supplementation are critical for favorable outcomes.
- Understanding acquired zinc deficiency is vital for managing complex pediatric nutritional cases.
Abstract:
We present a case of a transient acquired zinc deficiency in a breast-fed, 4-month-old-male prematurely born infant, with acrodermatitis enteropathica-like symptoms such as crusted, eroded, erythemato-squamous eruption in periorificial and acral patterns. The laboratory investigations showed low zinc levels in the infant's and the mother's serum and in the mother's milk; genetic analysis did not show any mutation in the SLC39A4 gene, involved in acrodermatitis enteropathica. Acquired zinc deficiency is often found in premature infants because of their increased requirement, the low serum and milk zinc levels in breastfeeding women being also an important risk factor, as in this case. A prompt zinc supplementation is essential for the good prognosis of the disease.
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