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Long-term follow-up and treatment in nine boys with X-linked creatine transporter defect
The creatine transporter (CRTR) defect is a recently discovered cause of X-linked intellectual disability for which treatment options have been explored. Creatine monotherapy has not proved effective, and the effect of treatment with L-arginine is still controversial. Nine boys between 8 months and...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249187/ https://www.ncbi.nlm.nih.gov/pubmed/21556832 http://dx.doi.org/10.1007/s10545-011-9345-1 |
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author | van de Kamp, Jiddeke M. Pouwels, Petra J. W. Aarsen, Femke K. ten Hoopen, Leontine W. Knol, Dirk L. de Klerk, Johannes B. de Coo, Ireneus F. Huijmans, Jan G. M. Jakobs, Cornelis van der Knaap, Marjo S. Salomons, Gajja S. Mancini, Grazia M. S. |
author_facet | van de Kamp, Jiddeke M. Pouwels, Petra J. W. Aarsen, Femke K. ten Hoopen, Leontine W. Knol, Dirk L. de Klerk, Johannes B. de Coo, Ireneus F. Huijmans, Jan G. M. Jakobs, Cornelis van der Knaap, Marjo S. Salomons, Gajja S. Mancini, Grazia M. S. |
author_sort | van de Kamp, Jiddeke M. |
collection | PubMed |
description | The creatine transporter (CRTR) defect is a recently discovered cause of X-linked intellectual disability for which treatment options have been explored. Creatine monotherapy has not proved effective, and the effect of treatment with L-arginine is still controversial. Nine boys between 8 months and 10 years old with molecularly confirmed CRTR defect were followed with repeated (1)H-MRS and neuropsychological assessments during 4–6 years of combination treatment with creatine monohydrate, L-arginine, and glycine. Treatment did not lead to a significant increase in cerebral creatine content as observed with H(1)-MRS. After an initial improvement in locomotor and personal-social IQ subscales, no lasting clinical improvement was recorded. Additionally, we noticed an age-related decline in IQ subscales in boys affected with the CRTR defect. |
format | Online Article Text |
id | pubmed-3249187 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-32491872012-01-11 Long-term follow-up and treatment in nine boys with X-linked creatine transporter defect van de Kamp, Jiddeke M. Pouwels, Petra J. W. Aarsen, Femke K. ten Hoopen, Leontine W. Knol, Dirk L. de Klerk, Johannes B. de Coo, Ireneus F. Huijmans, Jan G. M. Jakobs, Cornelis van der Knaap, Marjo S. Salomons, Gajja S. Mancini, Grazia M. S. J Inherit Metab Dis Original Article The creatine transporter (CRTR) defect is a recently discovered cause of X-linked intellectual disability for which treatment options have been explored. Creatine monotherapy has not proved effective, and the effect of treatment with L-arginine is still controversial. Nine boys between 8 months and 10 years old with molecularly confirmed CRTR defect were followed with repeated (1)H-MRS and neuropsychological assessments during 4–6 years of combination treatment with creatine monohydrate, L-arginine, and glycine. Treatment did not lead to a significant increase in cerebral creatine content as observed with H(1)-MRS. After an initial improvement in locomotor and personal-social IQ subscales, no lasting clinical improvement was recorded. Additionally, we noticed an age-related decline in IQ subscales in boys affected with the CRTR defect. Springer Netherlands 2011-05-10 2012 /pmc/articles/PMC3249187/ /pubmed/21556832 http://dx.doi.org/10.1007/s10545-011-9345-1 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Article van de Kamp, Jiddeke M. Pouwels, Petra J. W. Aarsen, Femke K. ten Hoopen, Leontine W. Knol, Dirk L. de Klerk, Johannes B. de Coo, Ireneus F. Huijmans, Jan G. M. Jakobs, Cornelis van der Knaap, Marjo S. Salomons, Gajja S. Mancini, Grazia M. S. Long-term follow-up and treatment in nine boys with X-linked creatine transporter defect |
title | Long-term follow-up and treatment in nine boys with X-linked creatine transporter defect |
title_full | Long-term follow-up and treatment in nine boys with X-linked creatine transporter defect |
title_fullStr | Long-term follow-up and treatment in nine boys with X-linked creatine transporter defect |
title_full_unstemmed | Long-term follow-up and treatment in nine boys with X-linked creatine transporter defect |
title_short | Long-term follow-up and treatment in nine boys with X-linked creatine transporter defect |
title_sort | long-term follow-up and treatment in nine boys with x-linked creatine transporter defect |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249187/ https://www.ncbi.nlm.nih.gov/pubmed/21556832 http://dx.doi.org/10.1007/s10545-011-9345-1 |
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