Steatocystoma Multiplex

A disorder characterized by multiple, wide spread cutaneous cysts that often become inflamed and rupture. It is caused by the same mutations in the gene coding for KRT-17 that are causative mutations for Pachyonychia congenita, Type 2. Natal teeth involvement is sometimes associated with steatocystoma multiplex.

Also Known As:

Multiple Sebaceous Cysts; Multiplex Steatocystoma; Sebaceous Cysts, Multiple; Cyst, Multiple Sebaceous; Cysts, Multiple Sebaceous; Multiple Sebaceous Cyst; Multiplex Steatocystomas; Sebaceous Cyst, Multiple; Steatocystoma Multiplices; Steatocystoma, Multiplex; Steatocystomas, Multiplex

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Skin Abnormalities: 159
    - Ectodermal Dysplasia: 505
      - Pachyonychia Congenita: 162
        Steatocystoma Multiplex: 49
- Inborn Genetic Diseases: 11939
  - Genetic Skin Diseases: 47
    - Ectodermal Dysplasia: 505
      - Pachyonychia Congenita: 162
        Steatocystoma Multiplex: 49
Skin and Connective Tissue Diseases
- Skin Diseases: 13127
  - Skin Abnormalities: 159
    - Ectodermal Dysplasia: 505
      - Pachyonychia Congenita: 162
        Steatocystoma Multiplex: 49
  - Nail Diseases: 101
    - Pachyonychia Congenita: 162
      - Steatocystoma Multiplex: 49
  - Genetic Skin Diseases: 47
    - Ectodermal Dysplasia: 505
      - Pachyonychia Congenita: 162
        Steatocystoma Multiplex: 49

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Disease

Drug/Important Bio-Agent (IBA)