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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)]. "