A case of Klinefelter syndrome with hypersexual desire

Kingsley Okolie, Sumathy Perampalam, Anthony Barker, Christopher Nolan

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Klinefelter syndrome (KS) is a chromosomal disorder affecting males, with the typical karyotype of 47, XXY due to a supernumerary X chromosome, which causes progressive testicular failure resulting in androgen deficiency and infertility. Despite it being the most common sex chromosomal disorder, its diagnosis is easily missed. In addition to its classical clinical features of tall stature, gynaecomastia, small testes, and symptoms and signs of hypogonadism including infertility, KS is also often associated with neurocognitive, behavioural and psychiatric disorders. We present a 44-year-old man with KS who, despite having erectile dysfunction, paradoxically had increased libido. He used sildenafil to overcome his erectile dysfunction. Hypersexuality was manifested by very frequent masturbation, multiple sexual partners most of whom were casual, and a sexual offence conviction at the age of 17 years. Discussion focuses on the frequent failure of clinicians to diagnose KS, the neurocognitive, behavioural and psychiatric aspects of KS, this unusual presentation of hypersexuality in a man with KS, and the challenges of medical management of hypogonadism in a man with a history of a sexual offence.
    Original languageEnglish
    Pages (from-to)1-5
    JournalEndocrinology, Diabetes & Metabolism Case Reports
    Volume2017
    Issue number1
    DOIs
    Publication statusPublished - 2017

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