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X linked ichthyosis (steroid sulphatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits.
  1. Lindsey Kent (lsk8{at}st-andrews.ac.uk)
  1. University of St Andrews, United Kingdom
    1. Jane Emerton (janeemerton{at}googlemail.com)
    1. University of Cambridge, United Kingdom
      1. Vishu Bhadravathi
      1. University of Cambridge, United Kingdom
        1. Emma Weisblatt (ejw44{at}cam.ac.uk)
        1. University of Cambridge, United Kingdom
          1. Greg Pasco (gp310{at}medschl.cam.ac.uk)
          1. University of Cambridge, United Kingdom
            1. Lionel R Willatt (lionel.willatt{at}addenbrookes.nhs.uk)
            1. Addenbrookes NHS Trust, United Kingdom
              1. Robert McMahon (rmcmahon{at}staffmail.ed.ac.uk)
              1. Addenbrookes NHS Trust, United Kingdom
                1. John R.W. Yates (jrwy1{at}cam.ac.uk)
                1. University of Cambridge, United Kingdom

                  Abstract

                  Background: X linked ichthyosis (XLI) (steroid sulphatase deficiency) is caused by deletions or point mutations of the steroid sulphatase (STS) gene on chromosome Xp22.32. Deletions of this region can be associated with cognitive behavioural difficulties including autism and animal work suggests the STS gene may be involved in attentional processes. We have therefore undertaken a systematic study of autism and Attention Deficit Hyperactivity Disorder (ADHD) in boys with XLI.

                  Methods: Cases of XLI were recruited from families originally ascertained when pregnancies with STS deficiency were identified through a routine maternal screening programme. Boys with XLI were assessed for ADHD and autism using standardised questionnaires and interviews. Deletions of the STS gene were identified and characterised by analysis of genomic DNA and/or fluorescent in-situ hybridization.

                  Results: 73% of families approached agreed to participate in the study. 25 boys with XLI were assessed for autism and ADHD. 40% fulfilled DSM-IV criteria for a diagnosis of ADHD, 80% of which were inattentive subtype. ADHD diagnoses were present in those with both deletions and presumed point mutations of STS. Additionally, 5 boys, from 3 unrelated families fulfilled criteria for an autistic spectrum disorder or related language / communication difficulty, and all had an unusually large deletion of the STS gene, which also encompassed the neuroligin 4 (NLGN4) gene. None of the boys with the typical deletion or presumed point mutations of STS demonstrated autistic difficulties.

                  Conclusions: STS deficiency may be a risk factor for ADHD with predominantly inattentive symptoms. Boys with XLI and large deletions encompassing STS and NLGN4 are at an increased risk of developing autism and related disorders

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