Frontiers in immunology · 2026
Acetylcholine receptor antibody-positive myasthenia gravis and Kennedy's disease overlap syndrome: a case report and literature review.
СтатьяКлинический случайОбзорНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Gao Guo-Hui, Xu Yu-Qing, Liu Yu-Dong, Liu Ying, Yuan Jing
Аннотация
OBJECTIVE: To investigate the clinical characteristics and electromyographic findings of a patient with acetylcholine receptor (AChR) antibody-positive myasthenia gravis (MG) overlapping with Kennedy's disease (KD), aiming to improve clinicians' recognition of this rare overlap syndrome and explore potential comorbid mechanisms.
METHODS: The clinical presentation, laboratory results, and neurophysiological features of one case with AChR antibody-positive MG and KD were analyzed. A literature review of MG overlapping with KD was performed.
CONCLUSION: Neurophysiological findings and androgen receptor gene testing results were consistent with a diagnosis of KD. Therefore, the patient was definitively diagnosed with overlap syndrome of AChR antibody-positive MG and KD. A literature review identified only four previously reported cases of KD patients exhibiting myasthenic features; however, all were AChR antibody-negative.
METHODS: The clinical presentation, laboratory results, and neurophysiological features of one case with AChR antibody-positive MG and KD were analyzed. A literature review of MG overlapping with KD was performed.
CONCLUSION: Neurophysiological findings and androgen receptor gene testing results were consistent with a diagnosis of KD. Therefore, the patient was definitively diagnosed with overlap syndrome of AChR antibody-positive MG and KD. A literature review identified only four previously reported cases of KD patients exhibiting myasthenic features; however, all were AChR antibody-negative.