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Results 51 - 60 of 64 for Autism spectrum disorder -epilepsy -arthrogryposis syndrome
  1. Alpha-N-acetylgalactosaminidase deficiency 
    ... seizures that begin in infancy; and features of autism spectrum disorder that appear in childhood. Autism spectrum disorder is characterized by impaired communication and socialization skills. ...
    https://medlineplus.gov/...lpha-n-acetylgalactosaminidase-deficiency - Genetics
  2. SLC6A3 gene 
    ... factors for attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD). ADHD, which typically begins in childhood, is ... the dopamine transporter gene associates dopamine dysfunction with autism spectrum disorder. Mol Psychiatry. 2013 Dec;18(12):1315-23. ...
    https://medlineplus.gov/genetics/gene/slc6a3 - Genetics
  3. Monoamine oxidase A deficiency 
    ... may have features of other neurodevelopmental disorders, including autism spectrum disorder and attention-deficit/hyperactivity disorder (ADHD). These features ...
    https://medlineplus.gov/.../condition/monoamine-oxidase-a-deficiency - Genetics
  4. MECP2 duplication syndrome 
    ... problems such as depression, anxiety, and features of autism spectrum disorder that affect communication and social interaction. Females with ...
    https://medlineplus.gov/.../condition/mecp2-duplication-syndrome - Genetics
  5. RERE gene 
    ... brain development, causing intellectual disability, delayed development, or autism spectrum disorder, which is a condition that affects communication and ...
    https://medlineplus.gov/genetics/gene/rere - Genetics
  6. Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart 
    ... motor skills (such as sitting and walking), or autism spectrum disorder, which is a condition that affects communication and ...
    https://medlineplus.gov/...thout-anomalies-of-the-brain-eye-or-heart - Genetics
  7. MAOA gene 
    ... have severe intellectual disability, difficulty with social interactions (autism spectrum disorders), and seizures in addition to features of Norrie ...
    https://medlineplus.gov/genetics/gene/maoa - Genetics
  8. Mucopolysaccharidosis type III 
    ... or aggressive. Some affected children display features of autism spectrum disorder, which is a condition characterized by difficulty with ... the natural course of mucopolysaccharidosis type IIIA (Sanfilippo syndrome type A). ... type C (MPS IIIC) disease in The Netherlands. Mol Genet Metab. 2008 Feb; ...
    https://medlineplus.gov/.../condition/mucopolysaccharidosis-type-iii - Genetics
  9. 1q21.1 microdeletion 
    ... this genetic change. These include developmental conditions called autism spectrum disorders that affect communication and social interaction, attention-deficit/ ...
    https://medlineplus.gov/genetics/condition/1q211-microdeletion - Genetics
  10. MIR17HG gene 
    ... stature. Affected individuals may also have features of autism spectrum disorder, which is characterized by impaired communication and social ...
    https://medlineplus.gov/genetics/gene/mir17hg - Genetics
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