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Zasp-Related Myofibrillar Myopathy

mutation in ZASP

Also Known As:

Myopathy, Myofibrillar, Zasp-Related; MFM, Zasp-related

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

Disease Context: Research Results

Musculoskeletal Diseases: 719
- Muscular Diseases: 10128
  - Atrophic Muscular Disorders: 320
    - Muscular Dystrophies: 5779
      - Zasp-Related Myofibrillar Myopathy: 1
Nervous System Diseases: 14178
- Neuromuscular Diseases: 2005
  - Muscular Diseases: 10128
    - Atrophic Muscular Disorders: 320
      - Muscular Dystrophies: 5779
        Zasp-Related Myofibrillar Myopathy: 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Muscular Dystrophies: 5779
    - Zasp-Related Myofibrillar Myopathy: 1

Related Diseases

1.	Distal Myopathies (Distal Muscular Dystrophy)
2.	Cardiomyopathies (Cardiomyopathy)

Experts

1.	Chen, Shuyun: 1 article (01/2017)
2.	Chen, Yunqing: 1 article (01/2017)
3.	Hong, Daojun: 1 article (01/2017)
4.	Zheng, Junjun: 1 article (01/2017)
5.	Zhu, Min: 1 article (01/2017)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Zasp-Related Myofibrillar Myopathy:

1.	Proteins (Proteins, Gene)FDA Link 01/01/2017 - "Mutations in the LDB3 gene have been identified in patients with Z-disc-associated, alternatively spliced, PDZ motif-containing protein (ZASP)-related myofibrillar myopathy (ZASP-MFM) characterized by late-onset distal myopathy with signs of cardiomyopathy and neuropathy. "