Acquired and Inherited Zinc Deficiency-Related Diseases in Children: A Case Series and a Narrative Review

Author:

Bellini Tommaso1ORCID,Bustaffa Marta1,Tubino Barbara1,Giordano Benedetta2,Formigoni Clelia2,Fueri Elena2,Casabona Federica2,Vanorio Barbara2,Pastorino Andrea2,Herzum Astrid3,Matucci-Cerinic Caterina4ORCID,Arrigo Serena5,Viglizzo Gianmaria3,Piccotti Emanuela1

Affiliation:

1. Pediatric Emergency Room and Emergency Medicine Unit, Emergency Department, IRCCS Istituto Giannina Gaslini, 16147 Genoa, Italy

2. Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal, and Child Health (DINOGMI), University of Genoa, 16132 Genoa, Italy

3. Dermatology Unit, IRCCS Istituto Giannina Gaslini, 16147 Genoa, Italy

4. Reumatology and Autoinflammatory Diseases Unit, IRCCS Istituto Giannina Gaslini, 16147 Genoa, Italy

5. Gastroenterology and Digestive Endoscopy Unit, IRCCS Istituto Giannina Gaslini, 16147 Genoa, Italy

Abstract

Zinc deficiency is a significant global health concern among children, manifesting in various acquired and inherited conditions. This comprehensive overview of acquired and inherited zinc deficiency-related diseases in children aimed to explore the clinical presentations, diagnostic challenges, and management strategies associated with these conditions. This case series elucidates the diverse clinical manifestations of zinc deficiency in pediatric patients, ranging from dermatitis and growth retardation to immune dysregulation and neurological abnormalities, and discusses the underlying genetic mechanisms, clinical phenotypes, and therapeutic interventions. The complexity of zinc deficiency-related diseases in children underscores the need for a multidisciplinary approach involving pediatricians, dermatologists, geneticists, and nutritionists to optimize patient care and outcomes.

Publisher

MDPI AG

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