Literature DB >> 12598825

Replacement of antipsychotic and antiepileptic medication by L-alpha-methyldopa in a woman with velocardiofacial syndrome.

James F O'Hanlon1, Rand C Ritchie, Edward A Smith, Rashiklal Patel.   

Abstract

We report the case of a 23-year-old woman with velocardiofacial syndrome (VCFS) and a history of psychosis and seizures. She had been treated with conventional antipsychotic and antiepileptic drugs for 10 and 3 years, respectively. However, she continued to experience occasional hallucinations and paroxysmal jerking of the extremities. L-alpha-methyldopa 500 mg b.i.d. (later reduced to 250 mg t.i.d.) was added to her regimen. Hallucinations and seizures stopped shortly. Over the course of approximately 1 year, the previous medications were discontinued without recurrence of psychotic and epileptic symptoms. Eventually, improved mental functions and behaviour enabled her transition from living in a licensed residential facility to sharing a private residence with a partner. VCFS is associated with haploinsufficiency of catecholamine-methyltransferase, leading to excessive extraneuronal catecholamine concentrations. Alpha-Methyldopa inhibits catecholamine neurotransmission in a variety of ways. It is possible that the drug compensated for genetically disturbed catecholamine transmission thus achieving beneficial effects in this case.

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Year:  2003        PMID: 12598825     DOI: 10.1097/00004850-200303000-00010

Source DB:  PubMed          Journal:  Int Clin Psychopharmacol        ISSN: 0268-1315            Impact factor:   1.659


  5 in total

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2.  Generalized Epilepsy and Myoclonic Seizures in 22q11.2 Deletion Syndrome.

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Review 3.  Velo-cardio-facial syndrome: 30 Years of study.

Authors:  Robert J Shprintzen
Journal:  Dev Disabil Res Rev       Date:  2008

Review 4.  22q11.2 Deletion Syndrome-Associated Parkinson's Disease.

Authors:  Erik Boot; Anne S Bassett; Connie Marras
Journal:  Mov Disord Clin Pract       Date:  2018-11-09

5.  Adverse effects of antipsychotic medication in patients with 22q11.2 deletion syndrome: A systematic review.

Authors:  Janna de Boer; Erik Boot; Lissa van Gils; Therese van Amelsvoort; Janneke Zinkstok
Journal:  Am J Med Genet A       Date:  2019-08-13       Impact factor: 2.802

  5 in total

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