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Results 1 - 10 of 105 for Cognitive disorders
  1. Sepiapterin reductase deficiency 
    ... reductase deficiency: a congenital dopa-responsive motor and cognitive disorder. Brain. 2005 Oct;128(Pt 10):2291-6. ...
    https://medlineplus.gov/.../sepiapterin-reductase-deficiency - Genetics
  2. VRK1 gene 
    ... Deep sequencing reveals 50 novel genes for recessive cognitive disorders. Nature. 2011 Sep 21;478(7367):57-63. ...
    https://medlineplus.gov/genetics/gene/vrk1 - Genetics
  3. CHOPS syndrome 
    ... abbreviation for a list of features of the disorder including cognitive impairment, coarse facial features, heart defects, obesity, lung ( ... development. Affected individuals have no history of the disorder in their family. ... Cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, ...
    https://medlineplus.gov/genetics/condition/chops-syndrome - Genetics
  4. Fragile XE syndrome 
    Fragile XE syndrome is a genetic disorder that impairs thinking ability and cognitive functioning. Most affected individuals have mild intellectual disability. In some people with this condition, cognitive function is described as borderline, which means ...
    https://medlineplus.gov/genetics/condition/fragile-xe-syndrome - Genetics
  5. DNMT1 gene 
    ... ear (sensorineural deafness), and excessive daytime sleepiness (narcolepsy). Cognitive decline occurs as the disorder progresses. Numbness, tingling, or pain in the arms ...
    https://medlineplus.gov/genetics/gene/dnmt1 - Genetics
  6. PGM3-congenital disorder of glycosylation 
    ... 3 Immunodeficiency 23 Immunodeficiency with hyper IgE and cognitive impairment Immunodeficiency-vasculitis-myoclonus syndrome PGM3 deficiency PGM3-CDG PGM3-related congenital disorder of glycosylation Phosphoglucomutase 3 deficiency Phosphoglucomutase deficiency type ...
    https://medlineplus.gov/...pgm3-congenital-disorder-of-glycosylation - Genetics
  7. Mitochondrial complex V deficiency 
    ... and coordination (ataxia). Many affected individuals also have cognitive impairment and an eye disorder called retinitis pigmentosa that causes vision loss.A ...
    https://medlineplus.gov/.../mitochondrial-complex-v-deficiency - Genetics
  8. AFF4 gene 
    ... abbreviation for a list of features of the disorder including cognitive impairment, coarse facial features, heart defects, obesity, lung ( ...
    https://medlineplus.gov/genetics/gene/aff4 - Genetics
  9. MED12 gene 
    ... unclear how these changes lead to the particular cognitive and physical features of the disorder. More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/med12 - Genetics
  10. MED13L gene 
    ... unclear how these changes lead to the particular cognitive and physical features of the disorder. More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/med13l - Genetics
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