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Results 1 - 10 of 32 for Specific language disorder
  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. Epilepsy-aphasia spectrum 
    ... in sleep FESD Focal epilepsies with speech and language disorders Focal epilepsy with speech disorder and with or ... New genes for focal epilepsies with speech and language disorders. Curr Neurol Neurosci Rep. 2015 Jun;15(6): ...
    https://medlineplus.gov/genetics/condition/epilepsy-aphasia-spectrum - Genetics
  3. Fragile X syndrome 
    ... individuals usually have delayed development of speech and language by age 2. ... focusing on specific tasks. About one-third of individuals with fragile ...
    https://medlineplus.gov/genetics/condition/fragile-x-syndrome - Genetics
  4. White-Sutton syndrome 
    ... syndrome is a disorder that causes intellectual disability, specific facial features, and other signs and symptoms affecting ... to be important to brain development, but the specific function of POGZ in the brain is not ...
    https://medlineplus.gov/genetics/condition/white-sutton-syndrome - Genetics
  5. SETBP1 haploinsufficiency disorder 
    ... the loss of SETBP1 protein leads to the specific features of SETBP1 haploinsufficiency disorder. A shortage of ... EE. Refining analyses of copy number variation identifies specific genes associated with developmental delay. Nat Genet. 2014 ...
    https://medlineplus.gov/.../setbp1-haploinsufficiency-disorder - Genetics
  6. Autosomal dominant epilepsy with auditory features 
    ... seizures. Some people hear more complex sounds, like specific voices or music, or changes in the volume ... or young adulthood. They may be triggered by specific sounds, such as a ringing telephone or speech, ...
    https://medlineplus.gov/...-dominant-epilepsy-with-auditory-features - Genetics
  7. CHMP2B-related frontotemporal dementia 
    ... Rossor M, Hardy J, Collinge J. Familial non-specific dementia maps to chromosome 3. Hum Mol Genet. ...
    https://medlineplus.gov/.../chmp2b-related-frontotemporal-dementia - Genetics
  8. Autism spectrum disorder 
    ... the activity of other genes or proteins.The specific ways that changes in these and other genes ... autism as a behavioral syndrome and not a specific mental disorder: Implications of genetic and phenotypic heterogeneity. ...
    https://medlineplus.gov/genetics/condition/autism-spectrum-disorder - Genetics
  9. Silver-Russell syndrome 
    ... in chromosome 11 that affect the regulation of specific genes. The genes that are thought to play ... disorder. However, the pattern of inheritance in a specific family depends on the exact genetic change and ...
    https://medlineplus.gov/genetics/condition/silver-russell-syndrome - Genetics
  10. Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 
    ... muscle, bone, and brain cells leads to the specific features of IBMPFD.In individuals with IBMPFD who ... condition may be caused by rare variants in specific genes or remain unknown. IBMPFD is sometimes known ...
    https://medlineplus.gov/...paget-disease-and-frontotemporal-dementia - Genetics
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