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My Son's Fight With a Mysterious Disease

机译:我儿子与神秘疾病的斗争

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Does it look to you like he's favoring one leg?" I asked our babysitter as my 8-year-old walked down the hall. Our perfectly healthy son, Vincent, began limping four years ago, and the limp never stopped. After pediatricians visits, hot baths and analgesics failed to erase the limp, we entered a limbo of diagnostic tests. It was the inspired hunch of the director of rheumatology at our local children's hospital that ended our anxious uncertainty with a mystery we could name: Fi-brodysplasia Ossificans Pro-gressiva, FOP for short, a rare genetic disorder that replaces muscle and connective tissue with bone.
机译:当我八岁的孩子走下大厅时,我问我们的保姆。我们完全健康的儿子文森特(Vincent)四年前开始行,the行从未停止。 ,热水澡和止痛药未能消除其mp行,我们进入了诊断测试的困境,这是我们当地儿童医院风湿病科主任的启发性直觉,以一种可以称为谜的方式结束了焦虑症的不确定性:Fi-brodysplasia Ossificans前侵,简称FOP,一种罕见的遗传疾病,用骨骼代替肌肉和结缔组织。

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