Results 1 - 6 of 6 for "16p11.2" deletion syndrome
  1. 16p11.2 deletion syndrome is a disorder caused by a deletion of a small piece of chromosome 16. The deletion ... at a location designated p11.2.People with 16p11.2 deletion syndrome usually have developmental delay and intellectual disability. Most ...
  2. ... structure or number of copies of chromosome 16. 16p11.2 deletion syndrome is caused by a deletion of about 600, ... the missing genes contribute to the features of 16p11.2 deletion syndrome, which include delayed development; intellectual disability; and autism ...
  3. Developmental Disabilities (National Library of Medicine)  
    Developmental disabilities are severe, long-term problems. They may be physical, such as blindness. They may affect mental ability, such as learning disabilities. ...
  4. Autism Spectrum Disorder (National Library of Medicine)  
    Autism spectrum disorder (ASD) is a neurological and developmental disorder that begins early in childhood and lasts throughout a person's life. It affects how ...
  5. ... can inherit the chromosomal change. 16p11.2 duplication syndrome 16p11.2 microduplication autism, susceptibility to, 14B AUTS14B Genetic Testing Registry: Chromosome 16p11.2 duplication syndrome 16p11.2 duplication Disease InfoSearch National Organization for Rare Disorders ( ...
  6. ... Métay C. Inherited 1q21.1q21.2 duplication and 16p11.2 deletion: a two-hit case with more severe clinical ...