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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 |
| Publicado: |
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 |