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Spinocerebellar ataxia 26

Also Known As:

SCA26 Spinocerebellar ataxia 26; Spinocerebellar ataxia type 26

Networked: 2 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Nervous System Diseases: 14178
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Nervous System Heredodegenerative Disorders: 63
    - Spinocerebellar Degenerations: 353
      - Spinocerebellar Ataxias: 2083
        Spinocerebellar ataxia 26: 2

Related Diseases

1.	Neurodevelopmental Disorders
2.	Hydrocephalus (Hydrocephaly)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Spinocerebellar ataxia 26:

1.

Peptide Elongation Factor 2 (EF-2)IBA

07/01/2022 - "A Comparison of Pathogenic Eukaryotic Elongation Factor 2 (EEF2) Variants in Spinocerebellar Ataxia 26 Versus De Novo Mutations."
08/01/2023 - "Heterozygous variants in EEF2, which encodes the elongation factor 2 (eEF2), have been associated to Spinocerebellar ataxia 26 (SCA26) and more recently to a childhood-onset neurodevelopmental disorder with benign external hydrocephalus. "