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Results 1 - 10 of 16 for Intellectual "disability," "X-linked" 45
  1. Snyder-Robinson syndrome 
    ... RE, Pegg AE. Spermine synthase deficiency resulting in X-linked intellectual disability (Snyder-Robinson syndrome). Methods Mol Biol. 2011;720:437-45. doi: 10.1007/978-1-61779-034-8_ ...
    https://medlineplus.gov/genetics/condition/snyder-robinson-syndrome - Genetics
  2. SMS gene 
    ... RE, Pegg AE. Spermine synthase deficiency resulting in X-linked intellectual disability (Snyder-Robinson syndrome). Methods Mol Biol. 2011;720:437-45. doi: 10.1007/978-1-61779-034-8_ ...
    https://medlineplus.gov/genetics/gene/sms - Genetics
  3. 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
  4. Partington syndrome 
    ... migration in the developing brain, leading to the intellectual disability and dystonia characteristic of Partington syndrome. ARX This condition is inherited in an X-linked recessive pattern. The gene associated with this condition ...
    https://medlineplus.gov/genetics/condition/partington-syndrome - Genetics
  5. 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
  6. Menkes syndrome 
    ... hypotonia), sagging facial features, seizures, developmental delay, and ... syndrome (sometimes called X-linked cutis laxa) is a less severe form of ...
    https://medlineplus.gov/genetics/condition/menkes-syndrome - Genetics
  7. CACNA1F gene 
    ... mutation has also been found to cause an X-linked retinal disorder in a large ... disability. The CACNA1F mutation associated with this condition alters ...
    https://medlineplus.gov/genetics/gene/cacna1f - Genetics
  8. Beta-propeller protein-associated neurodegeneration 
    ... Lennox-Gastaut syndrome.Children with BPAN also have intellectual disability, delayed development including significant problems with vocabulary and ... disorders. Some individuals who have been diagnosed with intellectual disability or early-onset parkinsonism based on their signs ...
    https://medlineplus.gov/...ller-protein-associated-neurodegeneration - Genetics
  9. Trichothiodystrophy 
    ... More severe cases also cause delayed development, significant intellectual disability, and recurrent infections; severely affected individuals may survive ...
    https://medlineplus.gov/genetics/condition/trichothiodystrophy - Genetics
  10. X chromosome 
    ... XXXY syndrome is a chromosomal condition that causes intellectual disabilities, developmental delays, physical differences, and an inability to ... XXXXY syndrome is a chromosomal condition that causes intellectual disabilities, developmental delays (especially in speech and language), changes ...
    https://medlineplus.gov/genetics/chromosome/x - Genetics
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