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A novel BBS10 mutation identified in a patient with Bardet-Biedl syndrome with a violent emotional outbreak.

Tatsuyuki OhtoTakashi EnokizonoRyuta TanakaMai TanakaHisato SuzukiAiko SakaiKazuo ImagawaHiroko FukushimaTakashi FukushimaRyo SumazakiTomoko UeharaToshiki TakenouchiKenjiro Kosaki
Published in: Human genome variation (2017)
We report a 10-year-old girl with Bardet-Biedl syndrome caused by a novel mutation in the Bardet-Biedl syndrome 10 (BBS10) gene. She had multiple malformations, including a dysmorphic face, postaxial polydactyly, polycystic kidney and amblyopia. She presented with typical BBS features, including intellectual disability with emotional outbursts and mild obesity. Whole-exome sequencing identified compound heterozygous mutations with NM_024685.3:c.1677C>A [p.(Tyr559*)] and c.1974T>G [p.(Tyr658*)]. To our knowledge, the latter mutation has never been reported previously.
Keyphrases
  • intellectual disability
  • case report
  • autism spectrum disorder
  • healthcare
  • metabolic syndrome
  • weight loss
  • insulin resistance
  • genome wide
  • photodynamic therapy
  • copy number
  • dna methylation
  • physical activity