HOME PRODUCTS COMPANY CONTACT FAQ

Research Dictionary Pharma

Sign Up FREE or Login

Spheroid body myopathy

Also Known As:

Autosomal dominant spheroid body myopathy

Networked: 6 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Musculoskeletal Diseases: 719
- Muscular Diseases: 10128
  - Congenital Structural Myopathies: 407
    - Spheroid body myopathy: 6
Nervous System Diseases: 14178
- Neuromuscular Diseases: 2005
  - Muscular Diseases: 10128
    - Congenital Structural Myopathies: 407
      - Spheroid body myopathy: 6

Related Diseases

1.	Muscular Diseases (Myopathy)
2.	Distal Myopathies (Distal Muscular Dystrophy)
3.	Myofibrillar Myopathy
4.	Limb-Girdle Muscular Dystrophies (Limb-Girdle Muscular Dystrophy)
5.	Myotilinopathy

Experts

1.	Dube, Dipak K: 1 article (09/2014)
2.	Dube, Syamalima: 1 article (09/2014)
3.	Fan, Yingli: 1 article (09/2014)
4.	Han, Mingda: 1 article (09/2014)
5.	Linask, Kersti: 1 article (09/2014)
6.	Pellenz, Christopher: 1 article (09/2014)
7.	Sanger, Jean M: 1 article (09/2014)
8.	Sanger, Joseph W: 1 article (09/2014)
9.	Wang, Jushuo: 1 article (09/2014)
10.	Hayashi, Yukiko: 1 article (01/2013)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Spheroid body myopathy:

1.	Proteins (Proteins, Gene)FDA Link 12/01/2023 - "Missense mutations in MYOT encoding the sarcomeric Z-disk protein myotilin cause three main myopathic phenotypes including proximal limb-girdle muscular dystrophy, spheroid body myopathy, and late-onset distal myopathy. " 09/01/2014 - "Several missense mutations in the Z-band protein, myotilin, have been implicated in human muscle diseases such as myofibrillar myopathy, spheroid body myopathy, and distal myopathy. " 12/01/2011 - "Protein aggregation in congenital myopathies may be encountered among different myofibrillar myopathies such as granulofilamentous myopathy, cytoplasmic body myopathy, or spheroid body myopathy, which are designated as αB crystallinopathy, desminopathy, and myotilinopathy, respectively, according to the respective mutant proteins. "
2.	DesminIBA 01/01/2013 - "Most of the diseases so-called desmin-related or storage myopathy, cytoplasmic body myopathy, spheroid body myopathy, reducing body myopathy, and hyaline body myopathy are included in MFM. " 06/01/2005 - "Spheroid body myopathy is a rare illness classified in the group of the congenital myopathies as a desmin-related neuromuscular disorder, presenting dominant autosomical origin with the beginning of the symptoms in the adult phase. " 05/01/1996 - "A number of myopathies whose common denominator is abnormal foci of desmin positivity have been described under the rubrics of spheroid body myopathy, cytoplasmic body myopathy, Mallory body myopathy, myopathy with granulofilamentous inclusions, desmin storage myopathy, and intermediate filament myopathy. "
3.	Mutant Proteins (Protein, Mutant)IBA 12/01/2011 - "Protein aggregation in congenital myopathies may be encountered among different myofibrillar myopathies such as granulofilamentous myopathy, cytoplasmic body myopathy, or spheroid body myopathy, which are designated as αB crystallinopathy, desminopathy, and myotilinopathy, respectively, according to the respective mutant proteins. "

Therapies and Procedures

1.	Denervation 06/01/2005 - "The muscle biopsy disclosed mixed standard to myopathy, denervation and inclusion bodies that are consistent to spheroid body myopathy. "