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Treatable inborn errors of metabolism presenting as cerebral palsy mimics: systematic literature review
BACKGROUND: Inborn errors of metabolism (IEMs) have been anecdotally reported in the literature as presenting with features of cerebral palsy (CP) or misdiagnosed as ‘atypical CP’. A significant proportion is amenable to treatment either directly targeting the underlying pathophysiology (often with...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273454/ https://www.ncbi.nlm.nih.gov/pubmed/25433678 http://dx.doi.org/10.1186/s13023-014-0197-2 |
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author | Leach, Emma L Shevell, Michael Bowden, Kristin Stockler-Ipsiroglu, Sylvia van Karnebeek, Clara DM |
author_facet | Leach, Emma L Shevell, Michael Bowden, Kristin Stockler-Ipsiroglu, Sylvia van Karnebeek, Clara DM |
author_sort | Leach, Emma L |
collection | PubMed |
description | BACKGROUND: Inborn errors of metabolism (IEMs) have been anecdotally reported in the literature as presenting with features of cerebral palsy (CP) or misdiagnosed as ‘atypical CP’. A significant proportion is amenable to treatment either directly targeting the underlying pathophysiology (often with improvement of symptoms) or with the potential to halt disease progression and prevent/minimize further damage. METHODS: We performed a systematic literature review to identify all reports of IEMs presenting with CP-like symptoms before 5 years of age, and selected those for which evidence for effective treatment exists. RESULTS: We identified 54 treatable IEMs reported to mimic CP, belonging to 13 different biochemical categories. A further 13 treatable IEMs were included, which can present with CP-like symptoms according to expert opinion, but for which no reports in the literature were identified. For 26 of these IEMs, a treatment is available that targets the primary underlying pathophysiology (e.g. neurotransmitter supplements), and for the remainder (n = 41) treatment exerts stabilizing/preventative effects (e.g. emergency regimen). The total number of treatments is 50, and evidence varies for the various treatments from Level 1b, c (n = 2); Level 2a, b, c (n = 16); Level 4 (n = 35); to Level 4–5 (n = 6); Level 5 (n = 8). Thirty-eight (57%) of the treatable IEMs mimicking CP can be identified by ready available metabolic screening tests in blood or urine, while the remaining IEMs require more specific and sometimes invasive tests. CONCLUSIONS: Limited by the rare nature of IEMs and incomplete information in the literature, we conclude that (1) A surprisingly large number of IEMs can present with CP symptoms, as ‘CP mimics’, (2) although individually rare, a large proportion of these diseases are treatable such that neurological damage can either be reversed or prevented, (3) clinician awareness of treatable CP mimics is important for appropriate screening, diagnosis, and early intervention, and (4) systematic studies are required to elucidate the collective frequency of treatable IEMs in CP. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13023-014-0197-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4273454 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42734542014-12-23 Treatable inborn errors of metabolism presenting as cerebral palsy mimics: systematic literature review Leach, Emma L Shevell, Michael Bowden, Kristin Stockler-Ipsiroglu, Sylvia van Karnebeek, Clara DM Orphanet J Rare Dis Research BACKGROUND: Inborn errors of metabolism (IEMs) have been anecdotally reported in the literature as presenting with features of cerebral palsy (CP) or misdiagnosed as ‘atypical CP’. A significant proportion is amenable to treatment either directly targeting the underlying pathophysiology (often with improvement of symptoms) or with the potential to halt disease progression and prevent/minimize further damage. METHODS: We performed a systematic literature review to identify all reports of IEMs presenting with CP-like symptoms before 5 years of age, and selected those for which evidence for effective treatment exists. RESULTS: We identified 54 treatable IEMs reported to mimic CP, belonging to 13 different biochemical categories. A further 13 treatable IEMs were included, which can present with CP-like symptoms according to expert opinion, but for which no reports in the literature were identified. For 26 of these IEMs, a treatment is available that targets the primary underlying pathophysiology (e.g. neurotransmitter supplements), and for the remainder (n = 41) treatment exerts stabilizing/preventative effects (e.g. emergency regimen). The total number of treatments is 50, and evidence varies for the various treatments from Level 1b, c (n = 2); Level 2a, b, c (n = 16); Level 4 (n = 35); to Level 4–5 (n = 6); Level 5 (n = 8). Thirty-eight (57%) of the treatable IEMs mimicking CP can be identified by ready available metabolic screening tests in blood or urine, while the remaining IEMs require more specific and sometimes invasive tests. CONCLUSIONS: Limited by the rare nature of IEMs and incomplete information in the literature, we conclude that (1) A surprisingly large number of IEMs can present with CP symptoms, as ‘CP mimics’, (2) although individually rare, a large proportion of these diseases are treatable such that neurological damage can either be reversed or prevented, (3) clinician awareness of treatable CP mimics is important for appropriate screening, diagnosis, and early intervention, and (4) systematic studies are required to elucidate the collective frequency of treatable IEMs in CP. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13023-014-0197-2) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-30 /pmc/articles/PMC4273454/ /pubmed/25433678 http://dx.doi.org/10.1186/s13023-014-0197-2 Text en © Leach et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Leach, Emma L Shevell, Michael Bowden, Kristin Stockler-Ipsiroglu, Sylvia van Karnebeek, Clara DM Treatable inborn errors of metabolism presenting as cerebral palsy mimics: systematic literature review |
title | Treatable inborn errors of metabolism presenting as cerebral palsy mimics: systematic literature review |
title_full | Treatable inborn errors of metabolism presenting as cerebral palsy mimics: systematic literature review |
title_fullStr | Treatable inborn errors of metabolism presenting as cerebral palsy mimics: systematic literature review |
title_full_unstemmed | Treatable inborn errors of metabolism presenting as cerebral palsy mimics: systematic literature review |
title_short | Treatable inborn errors of metabolism presenting as cerebral palsy mimics: systematic literature review |
title_sort | treatable inborn errors of metabolism presenting as cerebral palsy mimics: systematic literature review |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273454/ https://www.ncbi.nlm.nih.gov/pubmed/25433678 http://dx.doi.org/10.1186/s13023-014-0197-2 |
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