What is Acrodermatitis Enteropathica?
What is Acrodermatitis Enteropathica?
- Acrodermatitis Enteropathica: A rare inherited malabsorption disorder where the body is unable to absorb zinc in adequate quantities.
- Acrodermatitis Enteropathica: a severe human skin and gastrointestinal disease inherited as a recessive autosomal trait that is characterized by the symptoms of zinc deficiency and clears up when zinc is added to the diet.
Source - Diseases Database
Acrodermatitis Enteropathica is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Acrodermatitis Enteropathica, or a subtype of Acrodermatitis Enteropathica,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Acrodermatitis Enteropathica: Introduction
How serious is Acrodermatitis Enteropathica?
Complications of Acrodermatitis Enteropathica:
see complications of Acrodermatitis Enteropathica
What causes Acrodermatitis Enteropathica?
Causes of Acrodermatitis Enteropathica: see causes of Acrodermatitis Enteropathica
What are the symptoms of Acrodermatitis Enteropathica?
Symptoms of Acrodermatitis Enteropathica:
see symptoms of Acrodermatitis Enteropathica
Complications of Acrodermatitis Enteropathica:
see complications of Acrodermatitis Enteropathica
Acrodermatitis Enteropathica: Testing
Diagnostic testing: see tests for Acrodermatitis Enteropathica.
Misdiagnosis: see misdiagnosis and Acrodermatitis Enteropathica.
How is it treated?
Treatments for Acrodermatitis Enteropathica:
see treatments for Acrodermatitis Enteropathica
Research for Acrodermatitis Enteropathica:
see research for Acrodermatitis Enteropathica
Name and Aliases of Acrodermatitis Enteropathica
Main name of condition: Acrodermatitis Enteropathica
Other names or spellings for Acrodermatitis Enteropathica:
Brandt Syndrome, Danbolt-Cross Syndrome, Congenital Zinc deficiency, Acrodermatitis enteropathica zinc deficiency type, AEZ
AEZ, Acrodermatitis enteropathica zinc deficiency type
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)
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