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Type 1G Limb-Girdle Muscular Dystrophy

Also Known As:

Limb-Girdle Muscular Dystrophy, Type 1G; LGMD1G

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

Disease Context: Research Results

Musculoskeletal Diseases: 719
- Muscular Diseases: 10128
  - Atrophic Muscular Disorders: 320
    - Muscular Dystrophies: 5779
      - Limb-Girdle Muscular Dystrophies: 800
        Type 1G Limb-Girdle Muscular Dystrophy: 2
Nervous System Diseases: 14178
- Neuromuscular Diseases: 2005
  - Muscular Diseases: 10128
    - Atrophic Muscular Disorders: 320
      - Muscular Dystrophies: 5779
        Limb-Girdle Muscular Dystrophies: 800
        Type 1G Limb-Girdle Muscular Dystrophy: 2
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Muscular Dystrophies: 5779
    - Limb-Girdle Muscular Dystrophies: 800
      - Type 1G Limb-Girdle Muscular Dystrophy: 2

Related Diseases

1.	Limb-Girdle Muscular Dystrophies (Limb-Girdle Muscular Dystrophy)
2.	Type 1E Limb-Girdle Muscular Dystrophy
3.	Type 1D Limb-Girdle Muscular Dystrophy
4.	Type 1F Limb-Girdle Muscular Dystrophy
5.	Type 1C Limb-Girdle Muscular Dystrophy

Experts

1.	Nigro, Vincenzo: 2 articles (08/2014 - 05/2014)
2.	Cavaçana, Natale: 1 article (08/2014)
3.	Chuartzman, Silvia: 1 article (08/2014)
4.	Gal, Lihi: 1 article (08/2014)
5.	Kitajima, João Paulo: 1 article (08/2014)
6.	Kok, Fernando: 1 article (08/2014)
7.	Kunkel, Louis M: 1 article (08/2014)
8.	Licinio, Luciana: 1 article (08/2014)
9.	Mimbacas, Adriana: 1 article (08/2014)
10.	Naslavsky, Michel S: 1 article (08/2014)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Type 1G Limb-Girdle Muscular Dystrophy:

1.	Caveolin 3IBA 05/01/2014 - "The dominant forms (LGMD1) are: LGMD1A (myotilin), LGMD1B (lamin A/C), LGMD1C (caveolin 3), LGMD1D (DNAJB6), LGMD1E (desmin), LGMD1F (transportin 3), LGMD1G (HNRPDL), LGMD1H (chr. "
2.	Lamin Type A (Lamin A)IBA 05/01/2014 - "The dominant forms (LGMD1) are: LGMD1A (myotilin), LGMD1B (lamin A/C), LGMD1C (caveolin 3), LGMD1D (DNAJB6), LGMD1E (desmin), LGMD1F (transportin 3), LGMD1G (HNRPDL), LGMD1H (chr. "
3.	Karyopherins (Importin)IBA 05/01/2014 - "The dominant forms (LGMD1) are: LGMD1A (myotilin), LGMD1B (lamin A/C), LGMD1C (caveolin 3), LGMD1D (DNAJB6), LGMD1E (desmin), LGMD1F (transportin 3), LGMD1G (HNRPDL), LGMD1H (chr. "
4.	Proteins (Proteins, Gene)FDA Link 08/01/2014 - "A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G)."
5.	DesminIBA 05/01/2014 - "The dominant forms (LGMD1) are: LGMD1A (myotilin), LGMD1B (lamin A/C), LGMD1C (caveolin 3), LGMD1D (DNAJB6), LGMD1E (desmin), LGMD1F (transportin 3), LGMD1G (HNRPDL), LGMD1H (chr. "