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Due To Mecp2 Mutations Neonatal Severe Encephalopathy

Also Known As:

Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations; Mecp2-Related Severe Neonatal Encephalopathy

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

Disease Context: Research Results

Nervous System Diseases: 14178
- Neurologic Manifestations: 7102
  - Neurobehavioral Manifestations: 1586
    - Intellectual Disability: 8035
      - X-Linked Mental Retardation: 272
        Due To Mecp2 Mutations Neonatal Severe Encephalopathy: 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Nervous System Heredodegenerative Disorders: 63
    - X-Linked Mental Retardation: 272
      - Due To Mecp2 Mutations Neonatal Severe Encephalopathy: 1
  - X-Linked Genetic Diseases: 42
    - X-Linked Mental Retardation: 272
      - Due To Mecp2 Mutations Neonatal Severe Encephalopathy: 1

Experts

1.	Goji, Aya: 1 article (01/2018)
2.	Imoto, Issei: 1 article (01/2018)
3.	Ito, Hiromichi: 1 article (01/2018)
4.	Kagami, Shoji: 1 article (01/2018)
5.	Kohmoto, Tomohiro: 1 article (01/2018)
6.	Masuda, Kiyoshi: 1 article (01/2018)
7.	Mori, Tatsuo: 1 article (01/2018)
8.	Naruto, Takuya: 1 article (01/2018)
9.	Saito, Masako: 1 article (01/2018)
10.	Takahashi, Rizu: 1 article (01/2018)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Due To Mecp2 Mutations Neonatal Severe Encephalopathy:

1.	Protein Isoforms (Isoforms)IBA 01/01/2018 - "Mutations in MECP2 exon 1 affecting the MeCP2_e1 isoform are relatively rare causes of RTT in females, and only one case of a male patient with MECP2-related severe neonatal encephalopathy caused by a mutation in MECP2 exon 1 has been reported. "