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Case Reports
. 2021 Mar 20:2021:5523453.
doi: 10.1155/2021/5523453. eCollection 2021.

Obsessive-Compulsive Symptoms as a Manifestation of Homocystinuria

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Case Reports

Obsessive-Compulsive Symptoms as a Manifestation of Homocystinuria

Vera Froes et al. Case Rep Psychiatry. .

Abstract

Homocystinuria is a rare autosomal recessive metabolic disorder due to a defect in the cystathionine β-synthase (CBS) that leads to high homocysteine plasma levels. Psychiatric symptoms secondary to homocystinuria have been described in the literature; however, there is a lack of information about obsessive-compulsive symptoms correlated to this disorder. We describe the case of a 39 years old man, diagnosed with homocystinuria in childhood, with no previous psychiatric history that presented obsessive-compulsive disorder (OCD) like symptoms, as a manifestation of homocystinuria. This case underlines the importance for a psychiatrist to explore medical nonpsychiatric history, especially when presentation is abrupt, atypical, or in treatment-resistant cases.

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Conflict of interest statement

The authors declare that there are no conflicts of interest.

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References

    1. Sacharow S. J., Picker J. D., Levy H. L. In: Homocystinuria caused by cystathionine beta-synthase deficiency. Adam M. P., Ardinger H. H., Pagon R. A., editors. Seattle: GeneReviews®. Seattle (WA): University of Washington; 1993–2020. https://www.ncbi.nlm.nih.gov/books/NBK1524/ - PubMed
    1. Almuqbil M. A., Waisbren S. E., Levy H. L., Picker J. D. Revising the psychiatric phenotype of homocystinuria. Genetics in Medicine. 2019;21(8):1827–1831. doi: 10.1038/s41436-018-0419-4. - DOI - PubMed
    1. Abbott M. H., Folstein S. E., Abbey H., Pyeritz R. E., Opitz J. M. Psychiatric manifestations of homocystinuria due to cystathionine beta-synthase deficiency: prevalence, natural history, and relationship to neurologic impairment and vitamin B6-responsiveness. American Journal of Medical Genetics. 1987;26(4):959–969. doi: 10.1002/ajmg.1320260427. - DOI - PubMed
    1. Li S. C. H., Stewart P. M. Homocystinuria and psychiatric disorder: a case report. Pathology. 1999;31(3):221–224. doi: 10.1080/003130299105025. - DOI - PubMed
    1. Rahman T., Cole E. F. Capgras syndrome in homocystinuria. Biological Psychiatry. 2014;76(6):e11–e12. doi: 10.1016/j.biopsych.2013.11.026. - DOI - PubMed

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