疾病
医学
通气不足
基因检测
头痛
人口
束状
介绍(产科)
儿科
重症监护医学
精神科
外科
病理
内科学
麻醉
呼吸系统
环境卫生
作者
Helen Devine,Matthew R Solomons,Luca Zampedri,Michael G. Hanna,Carlo Rinaldi,Pietro Fratta,Dipa Jayaseelan
出处
期刊:Practical Neurology
[BMJ]
日期:2024-03-14
卷期号:24 (4): 302-305
标识
DOI:10.1136/pn-2023-004041
摘要
A 57-year-old man developed worsening early morning headaches, muscle cramps and falls over 12 months. He had widespread fasciculation and was diagnosed with motor neurone disease, and treated with nocturnal hypoventilation. Based on this diagnosis, he made significant personal and financial decisions including retiring and selling his house. He subsequently developed a lump in his right breast and was found to have gynaecomastia. This triggered genetic testing for Kennedy's disease leading to the correct diagnosis. This case highlights an unusual presentation of a rare disease leading to misdiagnosis and major repercussions for the patient. Recent genetic analysis from the 100 000 genome project suggests Kennedy's disease may be four times more prevalent in the population than previously thought, highlighting the need to consider genetic testing, especially if there is a suggestion of multisystem disease.
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