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Porokeratosis punctata palmaris et plantaris
Ppkp2 not included
Also Known As:
Keratoderma, Palmoplantar, Punctate Type Ii
Networked:
2
relevant articles (
0
outcomes,
0
trials/studies)
Disease Context: Research Results
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
Inborn Genetic Diseases: 11939
Genetic Skin Diseases: 47
Palmoplantar Keratoderma: 313
Porokeratosis punctata palmaris et plantaris: 2
Porokeratosis: 284
Porokeratosis punctata palmaris et plantaris: 2
Skin and Connective Tissue Diseases
Skin Diseases: 13127
Keratosis: 706
Palmoplantar Keratoderma: 313
Porokeratosis punctata palmaris et plantaris: 2
Porokeratosis: 284
Porokeratosis punctata palmaris et plantaris: 2
Genetic Skin Diseases: 47
Palmoplantar Keratoderma: 313
Porokeratosis punctata palmaris et plantaris: 2
Porokeratosis: 284
Porokeratosis punctata palmaris et plantaris: 2
Related Diseases
1.
Porokeratosis (Palmoplantar Porokeratosis)
2.
Neoplasms (Cancer)
Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to Porokeratosis punctata palmaris et plantaris:
1.
pneumococcal purpura-producing principle (PPPP)
IBA
06/01/1989 - "
Seven members from three generations of a Saudi family presented with porokeratosis punctata palmaris et plantaris (PPPP).
"
01/01/1997 - "
Cases of cancer-associated porokeratosis were collected from the European language literature and assigned to one of 5 different types [plaque type of Mibelli (PM); disseminated actinic superficial porokeratosis (DSAP); porokeratosis palmaris, plantaris et disseminata (PPPD); porokeratosis punctata palmaris et plantaris (PPPP); linear porokeratosis (LP)].
"