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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...

詳細記述

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書誌詳細
出版年:Cureus
主要な著者: Goyal, Chanan, Naqvi, Waqar, Sahu, Arti
フォーマット: Artigo
言語:Inglês
出版事項: Cureus 2020
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC7478925/
https://ncbi.nlm.nih.gov/pubmed/32923223
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.9622
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