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X-Linked Nonsyndromic Mental Retardation

Also Known As:

Mental Retardation, X-Linked Nonsyndromic

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
        X-Linked Nonsyndromic Mental Retardation: 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Nervous System Heredodegenerative Disorders: 63
    - X-Linked Mental Retardation: 272
      - X-Linked Nonsyndromic Mental Retardation: 1
  - X-Linked Genetic Diseases: 42
    - X-Linked Mental Retardation: 272
      - X-Linked Nonsyndromic Mental Retardation: 1

Related Diseases

1.	Duchenne Muscular Dystrophy (Muscular Dystrophy, Becker)

Experts

1.	Bhat, S S: 1 article (01/2006)
2.	DuPont, B R: 1 article (01/2006)
3.	Kim, K C: 1 article (01/2006)
4.	Ladd, S: 1 article (01/2006)
5.	Schmidt, K R: 1 article (01/2006)
6.	Schwartz, C E: 1 article (01/2006)
7.	Simensen, R J: 1 article (01/2006)
8.	Srivastava, A K: 1 article (01/2006)
9.	Stevenson, R E: 1 article (01/2006)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to X-Linked Nonsyndromic Mental Retardation:

1.	DystrophinIBA 01/01/2006 - "The three X chromosome aberrations in the patient include: a pericentric inversion (inv 1) that disrupted the Duchenne muscular dystrophy (DMD) gene, dystrophin, at Xp11.4; an Xq11.2q21.32 approximately q22.2 paracentric inversion (inv 2) putatively affecting no genes; and an interstitial deletion at Xq22.3 that results in functional nullisomy of several known genes, including a gene previously associated with X-linked nonsyndromic mental retardation, acyl-CoA synthetase long chain family member 4 (ACSL4). "
2.	Coenzyme A Ligases (Acid-Thiol Ligases)IBA 01/01/2006 - "The three X chromosome aberrations in the patient include: a pericentric inversion (inv 1) that disrupted the Duchenne muscular dystrophy (DMD) gene, dystrophin, at Xp11.4; an Xq11.2q21.32 approximately q22.2 paracentric inversion (inv 2) putatively affecting no genes; and an interstitial deletion at Xq22.3 that results in functional nullisomy of several known genes, including a gene previously associated with X-linked nonsyndromic mental retardation, acyl-CoA synthetase long chain family member 4 (ACSL4). "