Obsessive-Compulsive Symptoms as a Manifestation of Homocystinuria
- PMID: 33824770
- PMCID: PMC8007370
- DOI: 10.1155/2021/5523453
Obsessive-Compulsive Symptoms as a Manifestation of Homocystinuria
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.
Copyright © 2021 Vera Froes et al.
Conflict of interest statement
The authors declare that there are no conflicts of interest.
Similar articles
-
High prevalence of cerebral venous sinus thrombosis (CVST) as presentation of cystathionine beta-synthase deficiency in childhood: molecular and clinical findings of Turkish probands.Gene. 2014 Jan 25;534(2):197-203. doi: 10.1016/j.gene.2013.10.060. Epub 2013 Nov 6. Gene. 2014. PMID: 24211323
-
Enzyme replacement with PEGylated cystathionine β-synthase ameliorates homocystinuria in murine model.J Clin Invest. 2016 Jun 1;126(6):2372-84. doi: 10.1172/JCI85396. Epub 2016 May 16. J Clin Invest. 2016. PMID: 27183385 Free PMC article.
-
[A case report of pyridoxine-responsive homocystinuria].Med Pregl. 1999 Nov-Dec;52(11-12):501-4. Med Pregl. 1999. PMID: 10748775 Croatian.
-
Cystathionine β-synthase deficiency: Of mice and men.Mol Genet Metab. 2017 Jul;121(3):199-205. doi: 10.1016/j.ymgme.2017.05.011. Epub 2017 May 19. Mol Genet Metab. 2017. PMID: 28583326 Free PMC article. Review.
-
Classical homocystinuria: From cystathionine beta-synthase deficiency to novel enzyme therapies.Biochimie. 2020 Jun;173:48-56. doi: 10.1016/j.biochi.2019.12.007. Epub 2019 Dec 16. Biochimie. 2020. PMID: 31857119 Review.
Cited by
-
Hyperhomocysteinemia and Accelerated Aging: The Pathogenic Role of Increased Homocysteine in Atherosclerosis, Osteoporosis, and Neurodegeneration.Cureus. 2023 Jul 21;15(7):e42259. doi: 10.7759/cureus.42259. eCollection 2023 Jul. Cureus. 2023. PMID: 37605676 Free PMC article. Review.
References
-
- 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
-
- 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
Publication types
LinkOut - more resources
Full Text Sources
Other Literature Sources