2013-02-11
Kallmann syndrome and paranoid schizophrenia: A rare combination
Publication
Publication
Kallmann syndrome (KS) is a genetically heterogeneous and rare disorder characterised by the combination of hypothalamic hypogonadism and anosmia/hyposmia, a variable degree of intellectual disability and several somatic anomalies. In about one-third of the patients, mutations have been identified in at least seven different genes. Virtually no data are available about possible neuropsychiatric symptoms in KS. Here, a young adult male is described with a previous clinical diagnosis of KS and recent paranoid schizophrenia of which positive, but not negative symptoms, fully remitted upon treatment with antipsychotics. Neither genome-wide array analysis nor mutation analyses disclosed imbalances or mutations in any of presently known KS disease genes. This is the first report on a patient with KS and paranoid schizophrenia in whom extensive genetic analyses were performed. It is concluded that further studies are warranted in order to elucidate a possible increased risk for psychiatric symptoms in patients with KS.Copyright 2013 BMJ Publishing Group. All rights reserved.
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doi.org/10.1136/bcr-2012-007387, hdl.handle.net/1765/67294 | |
BMJ Case Reports | |
Organisation | Department of Psychiatry |
Verhoeven, W., Egger, J., Hovens, H., & Hoefsloot, L. (2013). Kallmann syndrome and paranoid schizophrenia: A rare combination. BMJ Case Reports. doi:10.1136/bcr-2012-007387 |