Arthrogryposis multiplex congenita is a rare neuromuscular condition characterized by limited movements and contractures of the hands and legs, along with scoliosis, while cognitive function remains normal; patients may require respiratory support such as BiPAP machines due to weak respiratory systems, and the condition often presents diagnostic challenges where doctors may classify it as an undefined neuromuscular disease when they cannot identify the exact cause.
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The Reality of an Undefined Diagnosis | The Majid Khan PodcastAdded:
arthrogryposis multiplex congenita. I know that's a very long name.
>> Mhm.
>> Uh but yeah, um so essentially I have limited movements and contractures of my main limbs, so my hands and my legs. And I've got scoliosis, which means my spine is not straight.
>> Mhm.
>> Uh along with my neck. Uh but other than that, my brain works fine.
Alhamdulillah. I've got weak immune system and respiratory system. So I require support, or certainly did, since 2016 on a BiPAP machine to help me with breathing at night.
It's a very rare condition, apparently, I'm told. And in fact, interestingly, when we came here in '07, the doctors actually said, "We can't even guarantee that you have this condition. They just call it often a undefined neuromuscular disease because they can't put their finger on exactly what it is."
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