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Darier Disease

More information in Books or onNLM PubMed
Definition: An autosomal dominantly inherited skin disorder characterized by warty malodorous papules that coalesce into plaques. It is caused by mutations in the ATP2A2 gene encoding SERCA2 protein, one of the SARCOPLASMIC RETICULUM CALCIUM-TRANSPORTING ATPASES. The condition is similar, clinically and histologically, to BENIGN FAMILIAL PEMPHIGUS, another autosomal dominant skin disorder. Both diseases have defective calcium pumps (CALCIUM-TRANSPORTING ATPASES) and unstable desmosomal adhesion junctions (DESMOSOMES) between KERATINOCYTES.      Other names Keratosis Follicularis; Darier-White Disease; Acrokeratosis Verruciformis of Hopf; Verruciformis, Acrokeratosis; Hopf Diseases; Hopf Acrokeratosis Verruciformis; Diseases, Hopf; Diseases, Darier-White; Disease, Hopf; Disease, Darier-White; Disease, Darier's; Disease, Darier; Dariers Disease; Darier-White Diseases; Darier White Disease; Hopf Disease; Darier's Disease; Acrokeratosis Verruciformis; Acantholytic Dyskeratotic Epidermal Nevus; Acantholytic Dyskeratotic Epidermal Nevi
 
SubstanceCAS Registry & nameCategoriesSource
Atrophodermia vermiculata  0   *Darier Disease.
Kyrle disease  0   *Corneal Opacity *Darier Disease.
Keratosis follicularis dwarfism cerebral atrophy  0   *Brain Diseases *Dwarfism *Darier Disease.

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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