| Literature DB >> 35698716 |
Danyon J Anderson1, Mokshal H Porwal1, Jay I Sandlow1.
Abstract
Angelman syndrome (AS) is a rare genetic imprinting disorder characterized by a maternal microdeletion of the 15q11q13 locus. It is traditionally associated with intellectual disability, inappropriate laughing, and a happy demeanor. Here, we report a patient with AS who presented with aggression and hypersexuality and was successfully treated with leuprolide injections for nine years until a definitive orchiectomy was performed. To the best of our knowledge, this is the first report of castration as a treatment for refractory behavioral symptoms in a patient with AS.Entities:
Keywords: aggression; angelman syndrome; hypersexuality; leuprolide; orchiectomy
Year: 2022 PMID: 35698716 PMCID: PMC9184178 DOI: 10.7759/cureus.24865
Source DB: PubMed Journal: Cureus ISSN: 2168-8184
Figure 1Pre- and post-injection total testosterone (ng/dL) and frequency of aggressive hypersexual symptoms (%).
Pre-injection total testosterone was taken before the first leuprolide dose. Post-injection total testosterone was taken after leuprolide doses (n = 3) to verify efficacy. The presence or absence of aggressive hypersexual symptoms (n = 17) was defined by the patient’s mother’s desire for further treatment of excessive masturbation, biting, scratching, and hitting.