Behavioural phenotype in Börjeson-Forssman-Lehmann syndrome

J Intellect Disabil Res. 2009 Apr;53(4):319-28. doi: 10.1111/j.1365-2788.2009.01156.x. Epub 2009 Feb 2.

Abstract

Background: Börjeson-Forssman-Lehmann syndrome (BFLs) is an X-linked inherited disorder characterised by unusual facial features, abnormal fat distribution and intellectual disability. As many genetically determined disorders are characterised not only by physical features but also by specific behaviour, we studied whether a specific behavioural phenotype exists in BFLs.

Methods: We studied in detail the behaviour of four molecularly proven BFLs patients, and reviewed available literature on BFLs specifically for behavioural characteristics.

Results: Behaviour in persons with BFLs is in general friendly, but can be challenging with externalising and thrill-seeking features. Social skills are good. However, variation among patients is wide. Three patients from a single family showed expressed hypersexual behaviour. This was not present in other patients.

Conclusion: In BFLs a specific behavioural phenotype exists and in behaviour general is challenging besides a friendly habit. Within single families more problematic behaviour may occur. Further behavioural and molecular analysis of a larger group of patients is warranted to determine whether a genotype-behavioural phenotype correlation exists.

Publication types

  • Case Reports

MeSH terms

  • Adipose Tissue*
  • Adolescent
  • Adult
  • Anxiety / complications
  • Anxiety / diagnosis
  • Anxiety / psychology
  • Body Height
  • Carrier Proteins / genetics
  • Chromosomes, Human, X / genetics*
  • Depression / complications
  • Depression / diagnosis
  • Depression / psychology
  • Diagnostic and Statistical Manual of Mental Disorders
  • Genetic Linkage / genetics
  • Genotype*
  • Humans
  • Intellectual Disability / complications
  • Intellectual Disability / genetics*
  • Male
  • Microcephaly*
  • Obesity / complications
  • Obesity / genetics*
  • Paraphilic Disorders / complications
  • Paraphilic Disorders / genetics*
  • Pedigree
  • Phenotype*
  • Point Mutation / genetics
  • Repressor Proteins
  • Syndrome
  • Young Adult

Substances

  • Carrier Proteins
  • PHF6 protein, human
  • Repressor Proteins