Literature DB >> 22749184

Neurotransmitter abnormalities and response to supplementation in SPG11.

Adeline Vanderver1, Davide Tonduti, Sarah Auerbach, Johanna L Schmidt, Sumit Parikh, Gordon C Gowans, Kelly E Jackson, Pamela L Brock, Marc Patterson, Michelle Nehrebecky, Rena Godfrey, Wadih M Zein, William Gahl, Camilo Toro.   

Abstract

OBJECTIVE: To report the detection of secondary neurotransmitter abnormalities in a group of SPG11 patients and describe treatment with l-dopa/carbidopa and sapropterin.
DESIGN: Case reports.
SETTING: National Institutes of Health in the Undiagnosed Disease Program; Children's National Medical Center in the Myelin Disorders Bioregistry Program. PATIENTS: Four SPG11 patients with a clinical picture of progressive spastic paraparesis complicated by extrapyramidal symptoms and maculopathy.
INTERVENTIONS: L-Dopa/carbidopa and sapropterin.
RESULTS: 3/4 patients presented secondary neurotransmitter abnormalities; 4/4 partially responded to L-dopa as well as sapropterin.
CONCLUSIONS: In the SPG11 patient with extrapyramidal symptoms, a trial of L-dopa/carbidopa and sapropterin and/or evaluation of cerebrospinal fluid neurotransmitters should be considered.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22749184      PMCID: PMC3517733          DOI: 10.1016/j.ymgme.2012.05.020

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  18 in total

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