Palmoplantar Keratoderma

Group of mostly hereditary disorders characterized by thickening of the palms and soles as a result of excessive keratin formation leading to hypertrophy of the stratum corneum (hyperkeratosis).

Also Known As:

Keratosis Palmaris et Plantaris; Keratosis, Palmoplantar; Meleda Disease; Keratoderma, Palmoplantar; Keratosis Palmoplantaris Transgradiens of Siemens; Mal de Meleda; Disease, Meleda; Keratodermas, Palmoplantar; Keratoses, Palmoplantar; Meleda, Mal de; Palmoplantar Keratodermas; Palmoplantar Keratoses; Palmoplantar Keratosis; de Meleda, Mal; Hyperkeratosis Palmaris et Plantaris

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Genetic Skin Diseases: 47
    - Palmoplantar Keratoderma: 313
Skin and Connective Tissue Diseases
- Skin Diseases: 13127
  - Keratosis: 706
    - Palmoplantar Keratoderma: 313
  - Genetic Skin Diseases: 47
    - Palmoplantar Keratoderma: 313

M Van Geel Selected Research

M Van Geel Research Topics

Disease

Drug/Important Bio-Agent (IBA)