autosomal dominant familial Periodic fever

An inherited condition characterized by recurrent episodes of FEVER; onset is typically in early childhood. Fevers usually persist for about three weeks, though they can be longer or shorter, and may not occur again for several weeks or several years. Other symptoms may include ABDOMINAL PAIN; MYALGIA; ARTHRALGIA; SKIN RASH and systemic INFLAMMATION; AMYLOIDOSIS may also occur in some cases. There is often no trigger, but episodes are sometimes preceded by infections, injury, or stress. Germline mutations in the TNFRSF1A gene have been identified. OMIM: 142680

Also Known As:

Periodic fever, familial, autosomal dominant; Autosomal Dominant Familial Periodic Fever; Familial Hibernian fever; Hibernian Familial Fever; Hibernian fever, familial; TNF Receptor-associated Periodic Syndrome (TRAPS); TNF receptor-associated periodic syndrome; Tumor necrosis factor receptor-associated periodic syndrome

Signs and Symptoms Pathological Conditions
- Signs and Symptoms
  - Body Temperature Changes: 152
    - Fever: 39160
      - autosomal dominant familial Periodic fever: 162
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Hereditary Autoinflammatory Diseases: 43
    - autosomal dominant familial Periodic fever: 162
Skin and Connective Tissue Diseases
- Skin Diseases: 13127
  - Genetic Skin Diseases: 47
    - Hereditary Autoinflammatory Diseases: 43
      - autosomal dominant familial Periodic fever: 162

Mischung,%20Claudia Selected Research

Mischung,%20Claudia Research Topics