HOME PRODUCTS COMPANY CONTACT FAQ

Research Dictionary Pharma

Sign Up FREE or Login

Spinocerebellar ataxia 27

Also Known As:

Cerebellar ataxia, autosomal dominant, FGF14-related; SCA27 Spinocerebellar ataxia 27

Networked: 5 relevant articles (0 outcomes, 1 trials/studies)

Disease Context: Research Results

Nervous System Diseases: 14178
- Neurodegenerative Diseases: 42472
  - Nervous System Heredodegenerative Disorders: 63
    - Spinocerebellar Degenerations: 353
      - Spinocerebellar ataxia 27: 5
- Central Nervous System Diseases: 4213
  - Brain Diseases: 15694
    - Cerebellar Diseases: 631
      - Spinocerebellar Degenerations: 353
        Spinocerebellar ataxia 27: 5
  - Spinal Cord Diseases: 4314
    - Spinocerebellar Degenerations: 353
      - Spinocerebellar ataxia 27: 5
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Nervous System Heredodegenerative Disorders: 63
    - Spinocerebellar Degenerations: 353
      - Spinocerebellar ataxia 27: 5

Related Diseases

1.	Tremor (Tremors)
2.	Ataxia (Dyssynergia)

Experts

1.	Alshammari, M: 1 article (01/2020)
2.	Alshammari, T: 1 article (01/2020)
3.	Bergendal, Å: 1 article (01/2020)
4.	Di Re, J: 1 article (01/2020)
5.	Granberg, T: 1 article (01/2020)
6.	Iwarsson, E: 1 article (01/2020)
7.	Laezza, F: 1 article (01/2020)
8.	Lindefeldt, M: 1 article (01/2020)
9.	Lundin, J: 1 article (01/2020)
10.	Paucar, M: 1 article (01/2020)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Spinocerebellar ataxia 27:

1.

fibroblast growth factor 14IBA

01/01/2020 - "The goal of this study was to characterize a Swedish family with members affected by spinocerebellar ataxia 27 (SCA27), a rare autosomal dominant disease caused by mutations in fibroblast growth factor 14 (FGF14). "
10/03/2023 - "ATX-FGF14 (formerly spinocerebellar ataxia 27, OMIM #193003) is an autosomal dominant condition caused by a pathogenic variant in the fibroblast growth factor 14 (FGF14, OMIM #601515) gene located on chromosome 13. "
11/15/2019 - "Fibroblast growth factor 14 (FGF14) is a functionally relevant component of the Nav1.6 channel complex, a causative link to spinocerebellar ataxia 27 (SCA27) and an emerging risk factor for neuropsychiatric disorders. "
03/01/2019 - "Spinocerebellar ataxia 27 (SCA27) is an autosomal dominant SCA caused by variants in the fibroblast growth factor 14 (FGF14) gene. "
01/01/2022 - "Spinocerebellar ataxia 27 (SCA 27) is a rare heredodegenerative disorder caused by mutations in the fibroblast growth factor 14 (FGF14) and characterized by early-onset tremor and progressive ataxia later during the disease course. "