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Results 1 - 8 of 8 for Specific language impairment 5
  1. FOXP2-related speech and language disorder 
    ... disorder is more complex and depends on the specific genetic change. Speech and language disorder with orofacial dyspraxia Speech-language disorder 1 Genetic ...
    https://medlineplus.gov/...oxp2-related-speech-and-language-disorder - Genetics
  2. Chromosome 7 
    ... Feuk L, Osborne LR, Scherer SW. Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2. Am J Med Genet A. 2006 Mar 1;140(5):509-14. doi: 10.1002/ajmg.a.31110. ...
    https://medlineplus.gov/genetics/chromosome/7 - Genetics
  3. Epilepsy-aphasia spectrum 
    ... New genes for focal epilepsies with speech and language disorders. Curr Neurol Neurosci Rep. 2015 Jun;15(6):35. doi: 10.1007/s11910-015-0554-0. Erratum In: Curr Neurol Neurosci Rep. 2015 Aug;15(8):55. doi: 10.1007/s11910-015-0578-5. Citation on PubMed
    https://medlineplus.gov/genetics/condition/epilepsy-aphasia-spectrum - Genetics
  4. Floating-Harbor syndrome 
    ... and affected individuals are usually among the shortest 5 percent of their ... and language impairment can lead to problems in verbal communication. Most ...
    https://medlineplus.gov/genetics/condition/floating-harbor-syndrome - Genetics
  5. Fragile X syndrome 
    ... ability to maintain attention and difficulty focusing on specific tasks. About ... of males and about 5 percent of females with fragile X syndrome.Most ...
    https://medlineplus.gov/genetics/condition/fragile-x-syndrome - Genetics
  6. Chromosome 17 
    ... factor is a protein that attaches (binds) to specific regions of DNA and helps control the activity ( ... normal development and function, its relationship to the specific features of Koolen-de Vries syndrome is unclear. ...
    https://medlineplus.gov/genetics/chromosome/17 - Genetics
  7. 15q11-q13 duplication syndrome 
    ... active) only on the maternal copy. This parent-specific gene activation results from a phenomenon called genomic ... of SUDEP. Epilepsy Behav. 2016 Aug;61:1-5. doi: 10.1016/j.yebeh.2016.04.001. ...
    https://medlineplus.gov/.../condition/15q11-q13-duplication-syndrome - Genetics
  8. Williams syndrome 
    ... the loss (deletion) of genetic material from a specific region of chromosome 7. The deleted region includes ... and behaviour. Nat Rev Neurosci. 2006 May;7(5):380-93. doi: 10.1038/nrn1906. Citation on ...
    https://medlineplus.gov/genetics/condition/williams-syndrome - Genetics