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About: Acrodermatitis enteropathica     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : umbel-rc:AilmentCondition, within Data Space : dbpedia.org associated with source document(s)

Type: ThingDiseaseyago:WikicatAutosomalRecessiveDisordersyago:WikicatCutaneousConditionsyago:WikicatMetabolicDisordersyago:WikicatMineralDeficienciesyago:Abstraction100002137yago:Attribute100024264yago:Condition113920835yago:Disease114070360yago:Disorder114052403yago:GeneticDisease114151139yago:IllHealth114052046yago:Illness114061805yago:Lack114449405yago:MetabolicDisorder114084502yago:MineralDeficiency114450172yago:Need114449126yago:PathologicalState114051917yago:PhysicalCondition114034177yago:WikicatGeneticDisordersdiseaseyago:State100024720umbel-rc:AilmentCondition New Facet based on Instances of this Class

Acrodermatitis enteropathica is an autosomal recessive metabolic disorder affecting the uptake of zinc through the inner lining of the bowel, the mucous membrane. It is characterized by inflammation of the skin (dermatitis) around bodily openings (periorificial) and the tips of fingers and toes (acral), hair loss (alopecia), and diarrhea. It can also be related to deficiency of zinc due to other, i.e. congenital causes. Other names for acrodermatitis enteropathica include Brandt syndrome and Danbolt–Cross syndrome.