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Porokeratosis

More information in Books or onNLM PubMed
Definition: A heritable disorder of faulty keratinization characterized by the proliferation of abnormal clones of KERATINOCYTES and lesions showing varying atrophic patches surrounded by an elevated, keratotic border. These keratotic lesions can progress to overt cutaneous neoplasm. Several clinical variants are recognized, including porokeratosis of Mibelli, linear porokeratosis, disseminated superficial actinic porokeratosis, palmoplantar porokeratosis, and punctate porokeratosis.  do not confuse with PARAKERATOSIS    Other names Porokeratosis, Punctate; Porokeratosis, Palmoplantar; Porokeratosis, Mibelli; Porokeratosis, Linear; Porokeratosis, Disseminated Superficial Actinic; Porokeratosis of Mibelli; Porokeratosis Palmaris et Plantaris Disseminata; Punctate Porokeratosis; Palmoplantar Porokeratosis; Mibelli Porokeratosis; Linear Porokeratosis; Type 2 Punctate PPK; Porokeratosis, Disseminated Superficial Actinic 2; Porokeratosis Plantaris Palmaris et Disseminata; Keratoderma Palmoplantar, Punctate Type 2; Disseminated Superficial Actinic Porokeratosis
 
SubstanceCAS Registry & nameCategoriesSource
Congenital facial linear porokeratosis  0   *Facial Dermatoses/congenital *Porokeratosis.
Craniosynostosis, anal anomalies, and porokeratosis  0   *Craniosynostoses *Digestive System Abnormalities *Porokeratosis Anal Canal/abnormalities.
Porokeratosis, disseminated superficial actinic 1  0   *Porokeratosis.
Porokeratosis punctata palmaris et plantaris  0   *Keratoderma, Palmoplantar *Porokeratosis. Arch. Derm. 1971;104: 682

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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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