Burnett Schwartz Berberian syndrome

Keratosis pilaris affecting the follicles of the eyebrow hairs

Also Known As:

Amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2; Atrophodermia Reticulata Symmetrica Faciei; Atrophodermia reticulata; Atrophodermia vermiculata; Folliculitis ulerythematosa; Folliculitis ulerythematosa reticulata; Honeycomb atrophy; Keratosis Pilaris Atrophicans Facies; Keratosis pilaris; Ulerythema ophryogenes; Ulerythema ophryogenes with multiple congenital anomalies; Ulerythema ophryogenesis

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Congenital Abnormalities: 26404
  - Multiple Abnormalities: 213
    - Burnett Schwartz Berberian syndrome: 105
- Inborn Genetic Diseases: 12342
  - Genetic Skin Diseases: 51
    - Darier Disease: 412
      - Burnett Schwartz Berberian syndrome: 105
Body Regions
- Head
  - Face
    - Eye
      - Eyebrows
        Burnett Schwartz Berberian syndrome: 105
Integumentary System
- Hair
  - Eyebrows
    - Burnett Schwartz Berberian syndrome: 105
Skin and Connective Tissue Diseases
- Skin Diseases: 13402
  - Keratosis: 712
    - Darier Disease: 412
      - Burnett Schwartz Berberian syndrome: 105
  - Genetic Skin Diseases: 51
    - Darier Disease: 412
      - Burnett Schwartz Berberian syndrome: 105

Wai Mun Sean Leong Selected Research

Wai Mun Sean Leong Research Topics

Disease

Drug/Important Bio-Agent (IBA)

Therapy/Procedure