Literature DB >> 1756605

Tuberous sclerosis in a child with de novo translocation t(3;12) (p26.3;q23.3).

R Fahsold1, H D Rott, U Claussen, B Schmalenberger.   

Abstract

We report on an 8-year-old boy with severe mental retardation, epileptic seizures, autistic behaviour, and X-ray CT findings of the skull characteristics for tuberous sclerosis. At the age of 9 years, first signs of adenoma sebaceum developed. Chromosomal analysis revealed a translocation t(3;12)(p26.3;q23.3). The parents were both healthy and had normal karyotypes. As non-random association of a chromosomal abnormality and tuberous sclerosis is hypothesized, a third locus for this disorder on 3p26 or 12q23 has to be taken in account.

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Year:  1991        PMID: 1756605     DOI: 10.1111/j.1399-0004.1991.tb03103.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  2 in total

1.  Linkage investigation of three putative tuberous sclerosis determining loci on chromosomes 9q, 11q, and 12q. The Tuberous Sclerosis Collaborative Group.

Authors:  J R Sampson; L A Janssen; L A Sandkuijl
Journal:  J Med Genet       Date:  1992-12       Impact factor: 6.318

2.  TSC loss distorts DNA replication programme and sensitises cells to genotoxic stress.

Authors:  Govind M Pai; Alexandra Zielinski; Dennis Koalick; Kristin Ludwig; Zhao-Qi Wang; Kerstin Borgmann; Helmut Pospiech; Ignacio Rubio
Journal:  Oncotarget       Date:  2016-12-20
  2 in total

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