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Results 1 - 7 of 7 for Childhood apraxia of speech
  1. FOXP2 gene 
    The FOXP2 gene provides instructions for making a protein that acts as a transcription factor, which means that it controls the activity of other genes. ...
    https://medlineplus.gov/genetics/gene/foxp2 - Genetics
  2. FOXP2-related speech and language disorder 
    ... childhood. Affected individuals have a condition known as childhood apraxia of speech (CAS), which makes it difficult to produce the ... dyspraxia Speech-language disorder 1 Genetic Testing Registry: Childhood apraxia of speech Isolated childhood apraxia of speech National Organization for ...
    https://medlineplus.gov/...oxp2-related-speech-and-language-disorder - Genetics
  3. SETBP1 haploinsufficiency disorder 
    ... percent of affected children have a condition called childhood apraxia of speech, in which they have difficulty with the mouth ...
    https://medlineplus.gov/.../setbp1-haploinsufficiency-disorder - Genetics
  4. 49,XXXXY syndrome 
    ... they are often diagnosed with a condition called childhood apraxia of speech. People with 49,XXXXY syndrome tend to be ...
    https://medlineplus.gov/genetics/condition/49xxxxy-syndrome - Genetics
  5. Down syndrome 
    ... 2016 Sep 8. Citation on PubMed Kumin L. Speech intelligibility and childhood verbal apraxia in children with Down syndrome. Downs Syndr Res ...
    https://medlineplus.gov/genetics/condition/down-syndrome - Genetics
  6. TPP1 gene 
    ... condition characterized by progressive problems with movement. During ... (oculomotor apraxia). People with SCAR7 have progressive loss of cells ( ...
    https://medlineplus.gov/genetics/gene/tpp1 - Genetics
  7. Ataxia-telangiectasia 
    ... difficulty with coordinating movements (ataxia) beginning in early ... apraxia). Small clusters of enlarged blood vessels called telangiectases, ...
    https://medlineplus.gov/genetics/condition/ataxia-telangiectasia - Genetics