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Type 1E Charcot-Marie-Tooth disease

Also Known As:

Charcot-Marie-Tooth disease, Type 1E

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
- Congenital Abnormalities: 25723
  - Nervous System Malformations: 35
    - Hereditary Sensory and Motor Neuropathy: 249
      - Charcot-Marie-Tooth Disease: 1019
        Type 1E Charcot-Marie-Tooth disease: 2
- Inborn Genetic Diseases: 11939
  - Nervous System Heredodegenerative Disorders: 63
    - Hereditary Sensory and Motor Neuropathy: 249
      - Charcot-Marie-Tooth Disease: 1019
        Type 1E Charcot-Marie-Tooth disease: 2

Related Diseases

1.	Peripheral Nervous System Diseases (PNS Diseases)

Experts

1.	Bai, Yunhong: 1 article (01/2017)
2.	Connolly, Anne M: 1 article (01/2017)
3.	Grider, Tiffany: 1 article (01/2017)
4.	Kamholz, John: 1 article (01/2017)
5.	Lupski, James R: 1 article (01/2017)
6.	Shy, Michael E: 1 article (01/2017)
7.	Wang, David S: 1 article (01/2017)
8.	Wu, Xingyao: 1 article (01/2017)
9.	Zaidman, Craig: 1 article (01/2017)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Type 1E Charcot-Marie-Tooth disease:

1.

Myelin ProteinsIBA

01/01/2022 - "Peripheral Myelin Protein 22 Gene Mutations in Charcot-Marie-Tooth Disease Type 1E Patients."
01/01/2017 - "To determine whether predicted fork stalling and template switching (FoSTeS) during mitosis deletes exon 4 in peripheral myelin protein 22 KD (PMP22) and causes gain-of-function mutation associated with peripheral neuropathy in a family with Charcot-Marie-Tooth disease type 1E. "