Autism in three patients with cystic or hyperechogenic kidneys and chromosome 17q12 deletion

Nephrol Dial Transplant. 2010 Oct;25(10):3430-3. doi: 10.1093/ndt/gfq380. Epub 2010 Jun 28.

Abstract

Background: We report autism in 3 out of 53 children with cystic or hyperechogenic kidneys and heterozygous 17q12 region deletion encompassing hepatocyte nuclear factor-1beta (HNF1B).

Results: They presented mental retardation, social interaction impairments, verbal and non-verbal communication deficits and stereotyped behaviours. Deletion size and location of breakpoints were similar to those reported in patients with renal disease/diabetes only.

Conclusion: Reciprocal genomic rearrangements of the 17q12 region, reported in patients with mental retardation and epilepsy, could also be involved in autism. Nephrologists should be aware of the possibility of autism in patients with 17q12 deletion including HNF1B locus.

Publication types

  • Case Reports

MeSH terms

  • Autistic Disorder / genetics*
  • Child
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 17*
  • Hepatocyte Nuclear Factor 1-beta / genetics*
  • Homeodomain Proteins / genetics
  • Humans
  • Kidney Diseases, Cystic / diagnostic imaging
  • Kidney Diseases, Cystic / genetics*
  • LIM-Homeodomain Proteins
  • Male
  • Transcription Factors
  • Ultrasonography

Substances

  • HNF1B protein, human
  • Homeodomain Proteins
  • LHX1 protein, human
  • LIM-Homeodomain Proteins
  • Transcription Factors
  • Hepatocyte Nuclear Factor 1-beta