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Results 1 - 10 of 12 for Multiple personality disorder
  1. Smith-Magenis syndrome 
    ... in each cell.Although the deleted region contains multiple genes, researchers believe that the loss of one ... phenotype correlation in Smith-Magenis syndrome: evidence that multiple genes in 17p11.2 contribute to the clinical ...
    https://medlineplus.gov/genetics/condition/smith-magenis-syndrome - Genetics
  2. C9orf72 gene 
    ... hexanucleotide repeat) can occur once or be repeated multiple times in a row; estimates suggest repeats of ... frontotemporal dementia (FTD), which is a progressive brain disorder that affects personality, behavior, and language. It is unclear why some ...
    https://medlineplus.gov/genetics/gene/c9orf72 - Genetics
  3. TARDBP gene 
    ... 156720511795563719. Citation on PubMed Buratti E, Baralle FE. Multiple roles of TDP-43 in gene expression, splicing ...
    https://medlineplus.gov/genetics/gene/tardbp - Genetics
  4. Huntington's disease 
    ... building blocks (cytosine, adenine, and guanine) that appear multiple times in a row. Normally, the CAG segment ...
    https://medlineplus.gov/genetics/condition/huntingtons-disease - Genetics
  5. Huntington's disease-like 
    ... genes contain a segment of DNA that repeats multiple times in a row. The variants that cause ...
    https://medlineplus.gov/genetics/condition/huntingtons-disease-like - Genetics
  6. ELN gene 
    ... provides instructions for making a protein called tropoelastin. Multiple copies of the tropoelastin protein attach to one ... people with Williams syndrome, which is a developmental disorder that is ... characteristics, distinctive facial features, and heart and blood ...
    https://medlineplus.gov/genetics/gene/eln - Genetics
  7. Thrombotic thrombocytopenic purpura 
    ... and symptoms, or, more commonly, they may experience multiple recurrences over time. The familial form of this ...
    https://medlineplus.gov/.../thrombotic-thrombocytopenic-purpura - Genetics
  8. Mowat-Wilson syndrome 
    ... and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations ...
    https://medlineplus.gov/genetics/condition/mowat-wilson-syndrome - Genetics
  9. Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 
    ... GD, Vesa J, Smith C, Kimonis VE. The multiple faces of valosin-containing protein-associated diseases: inclusion ...
    https://medlineplus.gov/...paget-disease-and-frontotemporal-dementia - Genetics
  10. FG syndrome 
    ... MJ, Stevenson RE. FG syndrome, an X-linked multiple congenital anomaly syndrome: the clinical phenotype and an ... 19. Citation on PubMed Lyons MJ. MED12-Related Disorders. 2008 ... FG syndrome: cognition, personality, and behavior in eleven affected boys. Am J ...
    https://medlineplus.gov/genetics/condition/fg-syndrome - Genetics
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