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Results 1 - 10 of 27 for Intellectual "disability," "X-linked" 21
  1. PPM-X syndrome 
    ... Genetic Testing Registry: Rett syndrome X-linked intellectual ... of MeCP2 deficiency. Nat Clin Pract Neurol. 2006 Apr;2(4):212-21. doi: 10.1038/ncpneuro0148. Citation on PubMed Gonzales ...
    https://medlineplus.gov/genetics/condition/ppm-x-syndrome - Genetics
  2. SMS gene 
    ... Mol Life Sci. 2010 Jan;67(1):113-21. doi: 10.1007/s00018-009-0165-5. Epub 2009 ... intellectual disability (Snyder-Robinson syndrome). Methods Mol Biol. 2011;720: ...
    https://medlineplus.gov/genetics/gene/sms - Genetics
  3. CASK-related intellectual disability 
    ... microcephaly with pontine and cerebellar hypoplasia (MICPCH), and X-linked intellectual disability (XL-ID) with or without nystagmus. Within each ... intellectual deficit, Najm type Genetic Testing Registry: Syndromic X-linked ... Najm type National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/.../cask-related-intellectual-disability - Genetics
  4. Snyder-Robinson syndrome 
    ... Spermine synthase deficiency SRS Genetic Testing Registry: Syndromic X-linked intellectual disability Snyder type X-linked intellectual disability, Snyder type ...
    https://medlineplus.gov/genetics/condition/snyder-robinson-syndrome - Genetics
  5. ARX gene 
    ... the X chromosome, this condition is known as X-linked intellectual disability (XLID) or sometimes nonsyndromic XLID. XLID can occur ... screening of ARX gene in Iranian families with X-linked intellectual disability. Arch Iran Med. 2012 Jun;15(6):361- ...
    https://medlineplus.gov/genetics/gene/arx - Genetics
  6. CASK gene 
    ... cerebellar hypoplasia (MICPCH), and a milder form called X-linked intellectual disability (XL-ID) with or without nystagmus.The mutations ...
    https://medlineplus.gov/genetics/gene/cask - Genetics
  7. HSD17B10 gene 
    ... in the HSD17B10 gene causes a form of X-linked intellectual disability called MRXS10. This disorder is characterized by intellectual ...
    https://medlineplus.gov/genetics/gene/hsd17b10 - Genetics
  8. Renpenning syndrome 
    ... 10.1074/jbc.M109.084525. Epub 2010 Apr 21. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/genetics/condition/renpenning-syndrome - Genetics
  9. MECP2-related severe neonatal encephalopathy 
    ... syndrome, which has signs and symptoms that include intellectual disability, seizures, ... of X-linked inheritance is that fathers cannot pass X-linked ...
    https://medlineplus.gov/...p2-related-severe-neonatal-encephalopathy - Genetics
  10. Coffin-Lowry syndrome 
    ... Coffin-Lowry syndrome typically have severe to profound intellectual disability and delayed development. Affected women may be cognitively normal, or they may have intellectual disability ranging from mild to profound. Beginning in childhood ...
    https://medlineplus.gov/genetics/condition/coffin-lowry-syndrome - Genetics
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