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Xia-Gibbs Syndrome: A Rare Case Report of a Male Child and Insight into Physiotherapy Management
Xia-Gibbs syndrome (XGS) is a recently discovered genetic disorder. It is characterized by global developmental delay, intellectual impairment, hypotonia, and sleep abnormalities. While the current literature emphasizes on the genotype and phenotype of this rare condition, it does not provide any de...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Cureus
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478925/ https://www.ncbi.nlm.nih.gov/pubmed/32923223 http://dx.doi.org/10.7759/cureus.9622 |
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author | Goyal, Chanan Naqvi, Waqar Sahu, Arti |
author_facet | Goyal, Chanan Naqvi, Waqar Sahu, Arti |
author_sort | Goyal, Chanan |
collection | PubMed |
description | Xia-Gibbs syndrome (XGS) is a recently discovered genetic disorder. It is characterized by global developmental delay, intellectual impairment, hypotonia, and sleep abnormalities. While the current literature emphasizes on the genotype and phenotype of this rare condition, it does not provide any description of the physiotherapy management of patients with XGS. We report a case of a 27-month-old Indian male diagnosed with XGS, who presented with difficulty in sitting without support. He had dysmorphic facies, hypotonia, hyperextensible joints, mild kyphoscoliosis, and global developmental delay. His parents and an elder female sibling were clinically asymptomatic. The physiotherapy intervention was based on the principles of neurodevelopmental treatment (NDT) and sensory integration (SI). The management included facilitation of transitions, weight-bearing exercises, wheelbarrow walking, joint compressions, rib cage mobilization, multidirectional reaching, and pushing-pulling activities along with the use of equipment like Swiss ball, balance board, stability disc, trampoline, swing system, walker (rollator), and walking harness. Also, stabilizing pressure input orthosis (SPIO) for the trunk and ankle-foot orthosis (AFO) followed by supramalleolar orthosis (SMO) were used for support. Thereafter, the child was able to stand and walk without support at the age of 36 months, and walk on uneven terrain at the age of 42 months. In addition, he could negotiate stairs using handrails with mild assistance. His gross motor function measure-88 (GMFM-88) total score improved from 21% at the presentation to 66.6% following the treatment. It was observed that the NDT and SI approaches along with the use of appropriate orthoses accelerated the achievement of motor milestones in this case. To the best of our knowledge, this is the first case report of a child with XGS that emphasizes on the course of physiotherapy management for the associated motor delay. |
format | Online Article Text |
id | pubmed-7478925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-74789252020-09-11 Xia-Gibbs Syndrome: A Rare Case Report of a Male Child and Insight into Physiotherapy Management Goyal, Chanan Naqvi, Waqar Sahu, Arti Cureus Neurology Xia-Gibbs syndrome (XGS) is a recently discovered genetic disorder. It is characterized by global developmental delay, intellectual impairment, hypotonia, and sleep abnormalities. While the current literature emphasizes on the genotype and phenotype of this rare condition, it does not provide any description of the physiotherapy management of patients with XGS. We report a case of a 27-month-old Indian male diagnosed with XGS, who presented with difficulty in sitting without support. He had dysmorphic facies, hypotonia, hyperextensible joints, mild kyphoscoliosis, and global developmental delay. His parents and an elder female sibling were clinically asymptomatic. The physiotherapy intervention was based on the principles of neurodevelopmental treatment (NDT) and sensory integration (SI). The management included facilitation of transitions, weight-bearing exercises, wheelbarrow walking, joint compressions, rib cage mobilization, multidirectional reaching, and pushing-pulling activities along with the use of equipment like Swiss ball, balance board, stability disc, trampoline, swing system, walker (rollator), and walking harness. Also, stabilizing pressure input orthosis (SPIO) for the trunk and ankle-foot orthosis (AFO) followed by supramalleolar orthosis (SMO) were used for support. Thereafter, the child was able to stand and walk without support at the age of 36 months, and walk on uneven terrain at the age of 42 months. In addition, he could negotiate stairs using handrails with mild assistance. His gross motor function measure-88 (GMFM-88) total score improved from 21% at the presentation to 66.6% following the treatment. It was observed that the NDT and SI approaches along with the use of appropriate orthoses accelerated the achievement of motor milestones in this case. To the best of our knowledge, this is the first case report of a child with XGS that emphasizes on the course of physiotherapy management for the associated motor delay. Cureus 2020-08-09 /pmc/articles/PMC7478925/ /pubmed/32923223 http://dx.doi.org/10.7759/cureus.9622 Text en Copyright © 2020, Goyal et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Neurology Goyal, Chanan Naqvi, Waqar Sahu, Arti Xia-Gibbs Syndrome: A Rare Case Report of a Male Child and Insight into Physiotherapy Management |
title | Xia-Gibbs Syndrome: A Rare Case Report of a Male Child and Insight into Physiotherapy Management |
title_full | Xia-Gibbs Syndrome: A Rare Case Report of a Male Child and Insight into Physiotherapy Management |
title_fullStr | Xia-Gibbs Syndrome: A Rare Case Report of a Male Child and Insight into Physiotherapy Management |
title_full_unstemmed | Xia-Gibbs Syndrome: A Rare Case Report of a Male Child and Insight into Physiotherapy Management |
title_short | Xia-Gibbs Syndrome: A Rare Case Report of a Male Child and Insight into Physiotherapy Management |
title_sort | xia-gibbs syndrome: a rare case report of a male child and insight into physiotherapy management |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478925/ https://www.ncbi.nlm.nih.gov/pubmed/32923223 http://dx.doi.org/10.7759/cureus.9622 |
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