Zinc Deficiency

ByLarry E. Johnson, MD, PhD, University of Arkansas for Medical Sciences
Reviewed/Revised Jul 2023
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    Zinc (Zn) is contained mainly in bones, teeth, hair, skin, liver, muscle, leukocytes, and testes. Zinc is a component of several hundred enzymes, including many nicotinamide adenine dinucleotide (NADH) dehydrogenases, RNA and DNA polymerases, and DNA transcription factors as well as alkaline phosphatase, superoxide dismutase, and carbonic anhydrase.

    (See also Overview of Mineral Deficiency and Toxicity.)

    A diet high in fiber and phytate (eg, in whole-grain bread) reduces zinc absorption.

    Dietary deficiency is unlikely in healthy persons. Secondary zinc deficiency can develop in the following:

    Maternal zinc deficiency may cause fetal malformations and low birth weight.

    Zinc deficiency in children causes impaired growth, impaired taste (hypogeusia) and smell, delayed sexual maturation, and hypogonadism and oligospermia in men. In children or adults, manifestations also include alopecia, impaired immunity, anorexia, dermatitis, night blindness, anemia, lethargy, and impaired wound healing. Zinc deficiency during pregnancy may result in a low birth weight and preterm birth.

    Clinicians should suspect zinc deficiency in undernourished patients based on typical symptoms or signs and their response to zinc supplements. However, because many of the symptoms and signs are nonspecific, clinical diagnosis of mild zinc deficiency is difficult. Biotin, riboflavin, and essential fatty acid deficiencies may resemble zinc deficiency. Laboratory diagnosis is also difficult, requiring special collection techniques. Low albumin levels, common in zinc deficiency, make serum zinc levels difficult to interpret; urine zinc levels are unreliable for acute deficiency, as are hair zinc levels. If available, isotope studies can measure zinc status more accurately.

    Treatment of zinc deficiency consists of elemental zinc 1 to 3 mg/kg orally once a day until symptoms and signs resolve.

    Acrodermatitis enteropathica

    Acrodermatitis enteropathica (a rare, once fatal autosomal recessive disorder) causes malabsorption of zinc. Psoriasiform dermatitis develops around the eyes, nose, and mouth; on the buttocks and perineum; and in an acral distribution. The disorder also causes hair loss, paronychia, impaired immunity, recurrent infection, impaired growth, and diarrhea. Symptoms and signs usually develop after infants are weaned from breast milk. In such cases, doctors suspect acrodermatitis enteropathica. If this diagnosis is correct, elemental zinc 1 to 3 mg/kg once a day orally usually results in complete remission.

    Zinc Deficiency
    Acrodermatitis Enteropathica With Perianal and Perineal Dermatitis
    Acrodermatitis Enteropathica With Perianal and Perineal Dermatitis

    Psoriasiform dermatitis can develop.

    © Springer Science+Business Media

    Acrodermatitis Enteropathica With Severe Perianal and Perineal Dermatitis
    Acrodermatitis Enteropathica With Severe Perianal and Perineal Dermatitis

    Psoriasiform dermatitis has progressed to local erythroderma.

    © Springer Science+Business Media

    Acrodermatitis Enteropathica With Paronychia
    Acrodermatitis Enteropathica With Paronychia

    Dermatitis can involve the nail folds and progress to paronychia.

    © Springer Science+Business Media

    Acrodermatitis Enteropathica in a Child
    Acrodermatitis Enteropathica in a Child

    Visible characteristic findings include hair loss and facial psoriasiform dermatitis.

    © Springer Science+Business Media

    Acrodermatitis Enteropathica With Severe Facial Dermatitis
    Acrodermatitis Enteropathica With Severe Facial Dermatitis

    © Springer Science+Business Media

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