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Results 1 - 9 of 9 for Intellectual "disability," "X-linked" 72
  1. X-linked intellectual disability, Siderius type 
    ... linked intellectual disability Siderius type X-linked intellectual disability, ... gene is associated with X-linked mental retardation with cleft lip/cleft palate. Clin Genet. 2007 Jul;72(1):19-22. doi: 10.1111/j.1399- ...
    https://medlineplus.gov/...ked-intellectual-disability-siderius-type - Genetics
  2. HSD17B10 gene 
    ... in the HSD17B10 gene causes a form of X-linked intellectual disability called MRXS10. This disorder is characterized by intellectual ...
    https://medlineplus.gov/genetics/gene/hsd17b10 - Genetics
  3. X-linked creatine deficiency 
    ... between 1 and 2 percent of males with intellectual disability. Variants (also known as mutations) in the SLC6A8 gene cause X-linked creatine deficiency. The SLC6A8 gene provides instructions for ...
    https://medlineplus.gov/.../condition/x-linked-creatine-deficiency - Genetics
  4. SLC6A8 gene 
    ... SLC6A8 gene have been identified in people with X-linked creatine deficiency, a disorder that causes intellectual disability, behavioral problems, seizures, and muscle weakness. SLC6A8 gene ...
    https://medlineplus.gov/genetics/gene/slc6a8 - Genetics
  5. HSD10 disease 
    ... of 1 and 2 and results in severe intellectual disability and loss of communication skills and motor skills ... disease may have developmental delay, learning problems, or intellectual disability, but they do not experience developmental regression. Some ...
    https://medlineplus.gov/genetics/condition/hsd10-disease - Genetics
  6. LAMP2 gene 
    ... muscle (cardiomyopathy), weakening of skeletal muscles (myopathy), and intellectual disabilities. The LAMP2 gene variants that cause Danon disease ...
    https://medlineplus.gov/genetics/gene/lamp2 - Genetics
  7. Mitochondrial complex I deficiency 
    ... as abnormal brain function (encephalopathy), recurrent seizures (epilepsy), intellectual disability, difficulty coordinating movements (ataxia), or involuntary movements (dystonia). ...
    https://medlineplus.gov/.../mitochondrial-complex-i-deficiency - Genetics
  8. SLC16A2 gene 
    ... the brain disrupts normal brain development, resulting in intellectual disability and problems with movement.If T3 is not ...
    https://medlineplus.gov/genetics/gene/slc16a2 - Genetics
  9. Charcot-Marie-Tooth disease 
    ... PubMed Wang Y, Yin F. A Review of X-linked Charcot-Marie-Tooth Disease. J Child Neurol. 2016 May;31(6):761-72. doi: 10.1177/0883073815604227. Epub 2015 Sep 18. ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics