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Noonan syndrome with somnambulism: A rare case report
Noonan syndrome is an autosomal dominant, genetic, multisystem disorder with a prevalence of 1 in 1000–2500 live births. Characteristic features of the condition include distinctive myopathic facial features, hypertelorism, short and broad nose, webbed neck, and low set ears. About 10% of the subjec...
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| 發表在: | Ind Psychiatry J |
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| Main Authors: | , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Wolters Kluwer - Medknow
2020
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8188914/ https://ncbi.nlm.nih.gov/pubmed/34158723 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ipj.ipj_84_19 |
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