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A novel BBS10 mutation identified in a patient with Bardet-Biedl syndrome with a violent emotional outbreak.
Ohto, Tatsuyuki; Enokizono, Takashi; Tanaka, Ryuta; Tanaka, Mai; Suzuki, Hisato; Sakai, Aiko; Imagawa, Kazuo; Fukushima, Hiroko; Fukushima, Takashi; Sumazaki, Ryo; Uehara, Tomoko; Takenouchi, Toshiki; Kosaki, Kenjiro.
Afiliação
  • Ohto T; Department of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
  • Enokizono T; Department of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
  • Tanaka R; Department of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
  • Tanaka M; Department of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
  • Suzuki H; Department of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
  • Sakai A; Department of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
  • Imagawa K; Department of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
  • Fukushima H; Department of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
  • Fukushima T; Department of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
  • Sumazaki R; Department of Pediatrics, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.
  • Uehara T; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
  • Takenouchi T; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
  • Kosaki K; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
Hum Genome Var ; 4: 17033, 2017.
Article em En | MEDLINE | ID: mdl-28808579
ABSTRACT
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_024685.3c.1677C>A [p.(Tyr559*)] and c.1974T>G [p.(Tyr658*)]. To our knowledge, the latter mutation has never been reported previously.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article