Familial Amyloid Neuropathies

Inherited disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. The different clinical types based on symptoms correspond to the presence of a variety of mutations in several different proteins including transthyretin (PREALBUMIN); APOLIPOPROTEIN A-I; and GELSOLIN.

Also Known As:

Familial Amyloid Polyneuropathy; Amyloid Neuropathies, Familial; Amyloid Neuropathy Type 1; Amyloid Polyneuropathy, British Type; Amyloid Polyneuropathy, Iowa Type; Amyloid Polyneuropathy, Swiss Type; Appalachian Type Familial Amyloid Polyneuropathy; British Type Amyloid Polyneuropathy; Cerebral Amyloid Angiopathy, British Type; Familial Amyloid Neuropathy, Andrade Type; Familial Amyloid Neuropathy, Finnish Type; Familial Amyloid Neuropathy, Portuguese Type; Familial Amyloid Polyneuropathy, Appalachian Type; Familial Amyloid Polyneuropathy, Jewish Type; Familial Amyloid Polyneuropathy, Type I; Familial Amyloid Polyneuropathy, Type II; Familial Amyloid Polyneuropathy, Type III; Familial Amyloid Polyneuropathy, Type IV; Familial Amyloid Polyneuropathy, Type V; Familial Amyloid Polyneuropathy, Type VI; Familial Portuguese Polyneuritic Amyloidosis; Finnish Type Familial Amyloid Neuropathy; Hereditary Neuropathic Amyloidosis; Iowa Type Amyloid Polyneuropathy; Jewish Type Familial Amyloid Polyneuropathy; Neuropathic Amyloid Syndrome; Polyneuritic Amyloidosis, Portuguese; Portuguese Polyneuritic Amyloidosis; Portuguese Type Familial Amyloid Neuropathy; Swiss Type Amyloid Polyneuropathy; Type I Familial Amyloid Polyneuropathy; Type II Familial Amyloid Polyneuropathy; Type III Familial Amyloid Polyneuropathy; Type IV Familial Amyloid Polyneuropathy; Type V Familial Amyloid Polyneuropathy; Type VI Familial Amyloid Polyneuropathy; Wohlwill-Andrade Syndrome; Wohlwill-Corino Andrade Syndrome; Amyloid Neuropathy, Familial; Amyloid Polyneuropathies, Familial; Amyloid Polyneuropathy, Familial; Amyloid Syndrome, Neuropathic; Amyloid Syndromes, Neuropathic; Amyloidoses, Hereditary Neuropathic; Amyloidoses, Portuguese Polyneuritic; Amyloidosis, Hereditary Neuropathic; Amyloidosis, Portuguese Polyneuritic; Familial Amyloid Neuropathy; Hereditary Neuropathic Amyloidoses; Neuropathic Amyloid Syndromes; Neuropathic Amyloidoses, Hereditary; Neuropathic Amyloidosis, Hereditary; Neuropathies, Familial Amyloid; Neuropathy, Familial Amyloid; Polyneuritic Amyloidoses, Portuguese; Polyneuropathies, Familial Amyloid; Polyneuropathy, Familial Amyloid; Portuguese Polyneuritic Amyloidoses; Wohlwill Andrade Syndrome; Wohlwill Corino Andrade Syndrome; Familial Amyloid Polyneuropathies

Nervous System Diseases: 14178
- Neurodegenerative Diseases: 42472
  - Nervous System Heredodegenerative Disorders: 63
    - Familial Amyloid Neuropathies: 656
- Neuromuscular Diseases: 2005
  - Peripheral Nervous System Diseases: 11383
    - Amyloid Neuropathies: 170
      - Familial Amyloid Neuropathies: 656
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
    - Familial Amyloidosis: 393
      - Familial Amyloid Neuropathies: 656
  - Nervous System Heredodegenerative Disorders: 63
    - Familial Amyloid Neuropathies: 656
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Proteostasis Deficiencies: 1400
    - Amyloidosis: 11630
      - Familial Amyloidosis: 393
        Familial Amyloid Neuropathies: 656
      - Amyloid Neuropathies: 170
        Familial Amyloid Neuropathies: 656
  - Inborn Errors Metabolism: 1162
    - Familial Amyloidosis: 393
      - Familial Amyloid Neuropathies: 656

Andrea Lautre Selected Research

Andrea Lautre Research Topics

Disease

Drug/Important Bio-Agent (IBA)