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Zinc Deficiency and Excess

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Encyclopedia of Molecular Mechanisms of Disease
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Definition and Characteristics

Zinc deficiency in humans was first recognized and characterized in 1963 [1]. Growth retardation due to zinc deficiency affecting children, adolescents, infants and fetuses, has been observed in many countries. Other manifestations of zinc deficiency include hypogonadism mainly affecting adolescent males, rough and dry skin, mental lethargy, poor appetite, delayed wound healing, frequent inter-current infections and abnormal neuro-sensory disorders. Acrodermatitis enteropathica (AE) that usually occurs in infants of Italian, Armenian or Iranian lineage is a lethal, autosomal, recessive trait disorder, caused by severe deficiency of zinc, resulting from genetically determined decreased zinc absorption. The gene for AE has now been characterized [2]. The clinical manifestation of AE includes bullous pustular dermatitis, blepheritis, conjunctivitis, corneal opacities, neuro-psychiatric disorders, weight loss, growth retardation, repeated severe...

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References

  1. Prasad AS, Miale A, Farid Z, Schulert A, Sandstead HH (1963) Zinc metabolism in patients with the syndrome of iron deficiency anemia, hypogonadism, and dwarfism. J Lab Clin Med 61:537–549

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  2. Wang K, Zhou B, Kuo YM, Zemansky J, Gitschier J (2002) A novel member of a zinc transporter family is defective in acrodermatitis enteropathica. Am J Hum Genet 71(1):66–73

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  4. Prasad AS (1993) Biochemistry of zinc. Plenum Press, New York

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  5. Prasad AS (2000) Effects of zinc deficiency on Th1 and Th2 cytokine shifts. J Inf Dis 182:S62–S68

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© 2009 Springer-Verlag GmbH Berlin Heidelberg

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Prasad, A.S. (2009). Zinc Deficiency and Excess. In: Lang, F. (eds) Encyclopedia of Molecular Mechanisms of Disease. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-29676-8_1912

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