Acrodermatitis enteropathica is an autosomal recessive disorder characterized by periorificial (around the natural orifices) and acral (in the limbs) dermatitis, alopecia (loss of hair), and diarrhea. Similar features may be present in acquired zinc deficiency. This disease also is related to deficiency of zinc due to congenital causes.
Some synonyms of this condition are:
- Brandt Syndrome
- Danbolt-Cross Syndrome
- Congenital Zinc Deficiency
Pathogenesis
The genetic
mutation of SLC39A4 gene on
Chromosome 8q
locus 24.3 appears to be the cause. The SLC39A4 gene appears to encode a
transmembrane protein that serves as a zinc uptake protein. The features of the disease usually start manifesting as an infant is weaned from breast milk. This has led some scientists to suspect that human milk contains a beneficial substance that helps uptake of
zinc and prevents the disease from being manifested while an infant is on breast milk.
Presentation
Features of acrodermatitis enteropathica start appearing in the first few months of life, as the infant discontinues breast milk. There are
erythematous patches and
plaques of dry, scaly skin. The lesions may appear
eczematous, or may evolve further into crusted
vesicles ,
bullas or
pustules. The lesions are frequent around natural orifices like the mouth (peri-oral) and anus (peri-anal), and also in hands, feet and
scalp.
There may be
suppurative inflammation of the
nail fold surrounding the
nail plate - known as
paronychia.
Alopecia - loss of hair from scalp, eyebrows and eyelashes may occur. The skin lesions may be secondarily infected by
bacteria such as
Staphylococcus aureus or
fungi like
Candida albicans. These skin lesions are accompanied by diarrhea.
Treatment
Without treatment, the disease is fatal and affected individuals may die within a few years. However, there is no absolute treatment of the condition. Lifelong dietary
zinc supplementation in the range of greater than 1-2
mg/
kg of bodyweight per day is usually needed.
External links
Organizations and resources
The following organizations provide information and patient support resources:
Congenital disorders | Gastroenterology | Genetic disorders | Dermatology
Acrodermatitis enteropathica