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Results 1 - 10 of 11 for Speech apraxia
  1. FOXP2-related speech and language disorder 
    ... disorder 1 Genetic Testing Registry: Childhood apraxia of speech Isolated childhood apraxia of speech National Organization for Rare Disorders (NORD) SPEECH-LANGUAGE ...
    https://medlineplus.gov/...oxp2-related-speech-and-language-disorder - Genetics
  2. 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
  3. SETBP1 haploinsufficiency disorder 
    ... 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 
    ... 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. Ataxia-telangiectasia 
    ... adolescence. People with this disorder also have slurred speech and trouble moving their eyes to look side-to-side (oculomotor apraxia). Small clusters of enlarged blood vessels called telangiectases, ...
    https://medlineplus.gov/genetics/condition/ataxia-telangiectasia - Genetics
  7. TPP1 gene 
    ... childhood, individuals with SCAR7 develop walking difficulties; impaired speech ... (oculomotor apraxia). People with SCAR7 have progressive loss of cells ( ...
    https://medlineplus.gov/genetics/gene/tpp1 - Genetics
  8. Snijders Blok-Campeau syndrome 
    ... only a few words or never speak. If speech occurs, it usually develops after ... to form words (apraxia). In general, people with this condition have a ...
    https://medlineplus.gov/.../condition/snijders-blok-campeau-syndrome - Genetics
  9. PNKP gene 
    ... microcephaly), recurrent seizures (epilepsy), and delayed development of ... with oculomotor apraxia type 4 (described above), the repair of double- ...
    https://medlineplus.gov/genetics/gene/pnkp - Genetics
  10. GRN-related frontotemporal lobar degeneration 
    ... speaking, remembering words and names (dysnomia), and understanding speech. Over ... The prevalence of GRN-related frontotemporal lobar degeneration ...
    https://medlineplus.gov/...related-frontotemporal-lobar-degeneration - Genetics
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