Aa
Question about Hereditary Spastic Paraplegia
Here's my quick history: paralyzed about 14 years ago, due to what they told me was transverse myelitis (no lesions showed up at the time, if I recall correctly). I mostly recovered, though with some gait problems and unable to run very fast.
Everything was fine for a long time, until about 7 years ago I started having temperature dysregulation problems. Constantly feeling hot, and sweating excessively. It started off mild but has gotten really bad. Then about 3 years ago, the spasticity in my legs started getting worse, and it's gotten pretty bad by now as well. Most recently, I've been getting dizzy headaches off and on, which are somewhat mild, but make it very hard to get work done. I've done all the MRIs, with contrast and without, and nothing showed up. EMGs, EPs, and other tests all negative (and thyroid problems have been ruled out). Still waiting on my lumbar puncture results.
I have a parent with neurological problems (not sure exactly of what the diagnosis was, but I'm told it was a demyelinating disease other than MS). So my neurologist suspects Hereditary Spastic Paraplegia. I'll be getting those genetic tests soon, though if I understand correctly, those tests miss a lot because it could be one of many genes that are affected.
My question: is this a strange pattern for HSP? Why would I have become paralyzed first, and then be fine for a while, before developing the HSP symptoms?
Everything was fine for a long time, until about 7 years ago I started having temperature dysregulation problems. Constantly feeling hot, and sweating excessively. It started off mild but has gotten really bad. Then about 3 years ago, the spasticity in my legs started getting worse, and it's gotten pretty bad by now as well. Most recently, I've been getting dizzy headaches off and on, which are somewhat mild, but make it very hard to get work done. I've done all the MRIs, with contrast and without, and nothing showed up. EMGs, EPs, and other tests all negative (and thyroid problems have been ruled out). Still waiting on my lumbar puncture results.
I have a parent with neurological problems (not sure exactly of what the diagnosis was, but I'm told it was a demyelinating disease other than MS). So my neurologist suspects Hereditary Spastic Paraplegia. I'll be getting those genetic tests soon, though if I understand correctly, those tests miss a lot because it could be one of many genes that are affected.
My question: is this a strange pattern for HSP? Why would I have become paralyzed first, and then be fine for a while, before developing the HSP symptoms?
Hi, I have HSP as well. The frequent urinary urges is pertty usual with HSP. Since you have spaticity in your legs, having it with your bladder is not uncommon: so do I. Your headaches is something I can comment on as well. I regularly have Migraines which average 14 per month based on last year's figures. Nerves are areal Pain! Baclofin as well as Nuerontin can be benefical in helping control the spasticity. Since there are as many as 24 variable sites, genetic testing is a waste of time and money. There is an organization which maybe be of more help. This is the Spastic Paraplegia Foundation Inc. Here is there web site address: www.sp-foundation. org . If you would like to get in touch with me, my e-mail add is gvanness_7458***@****. Hope this has been of some help; hang in there beleive me there are worst cases out there, I have seen them.
No, especially after several year you are expected to have some type weakness/paralysis but the dominant featue is spasticity of the legs
Generally ,If muscle weakness is present, it usually involves iliopsoas muscle (flexion of th hip), tibialis anterior (dorsiflexion of the foot), and, to a lesser extent, the hamstring muscles (bending the knee).
Take care
Bob
Generally ,If muscle weakness is present, it usually involves iliopsoas muscle (flexion of th hip), tibialis anterior (dorsiflexion of the foot), and, to a lesser extent, the hamstring muscles (bending the knee).
Take care
Bob
Well I certainly have the gait problems and hyperreflexia (along with the other problems I mentioned).
Is the paralysis so out of character with HSP as to make it very unlikely, or do we just not know enough about HSP to say with any certainty?
By the way, the LP's came back negative as well.
Is the paralysis so out of character with HSP as to make it very unlikely, or do we just not know enough about HSP to say with any certainty?
By the way, the LP's came back negative as well.
First of all, keep in mind that I am unable to diagnose you because I am unable to examine you, this forum is for educational purposes. The symptoms and story you describe is odd for Hereditary Spastic Paraplegia. This condition generally presents with variable progressive gait problems that finally end in paralysis, not a sudden transient paralysis that then resolves partially. Your story is indeed more consistent with a transvere myelitis or spinal cord injury of some kind (vascular or inflammatory). It sounds like you have had the right tests and I would also recommend the genetic testing, since there are always new variants being discovered. I would make sure that your evoked potentials were done on the lower extremity and the upper extremity (the lower is abnormal in HSP, but the upper is often normal). With your current symptoms of dizziness and headaches, I would make sure they have evaluated your posterior circulation blood vessels. Veterbro-basilar insufficiency can cause transient paralysis, gait problems and dizziness, headaches. An MRA (Magnetic resonance angiogram) would be a place to start, but you may need a formal cerebral angiogram.
I hope this has been helpful.
I hope this has been helpful.
I also forgot to say I'm a 27 year old male
Hi
I will begin by saying that the diagnosis of HSP is a diagnosis of exclusion , meaning the other disorders that cause similar picture should be excluded by detailed investigations, and I'm sure your doctor did that. I'm not sure if genetic testing is available for the few abnormal genes out of the research media?
Any way, HSP is divided to
1- Pure type were only spastic lower limb picture like you but some reports mentioned that you may get bladder problem and some sensory complaints.
2- Complicated type were the person may get any other neurological symptomes and usually starts at a later age (after 30)
The obligatory criteria suggested for the diagnosis of pure HSP includes:
1-positive family history if of a dominant inheritance only
2-progressive gait disturbance, spasticity of the lower limbs, and hyperreflexia of the lower limbs.
3- The most important is "Gait disturbance progresses slowly without exacerbations, remissions, or worsenings" so what happened 14 years ago were weakness was the dominant feature and was sudden is not in keeping with HSP and could be a different entity though if it was months apart we could think of infectious causes or even autoimmune diseases
Regards,
Bob
I will begin by saying that the diagnosis of HSP is a diagnosis of exclusion , meaning the other disorders that cause similar picture should be excluded by detailed investigations, and I'm sure your doctor did that. I'm not sure if genetic testing is available for the few abnormal genes out of the research media?
Any way, HSP is divided to
1- Pure type were only spastic lower limb picture like you but some reports mentioned that you may get bladder problem and some sensory complaints.
2- Complicated type were the person may get any other neurological symptomes and usually starts at a later age (after 30)
The obligatory criteria suggested for the diagnosis of pure HSP includes:
1-positive family history if of a dominant inheritance only
2-progressive gait disturbance, spasticity of the lower limbs, and hyperreflexia of the lower limbs.
3- The most important is "Gait disturbance progresses slowly without exacerbations, remissions, or worsenings" so what happened 14 years ago were weakness was the dominant feature and was sudden is not in keeping with HSP and could be a different entity though if it was months apart we could think of infectious causes or even autoimmune diseases
Regards,
Bob
Oh, also, I have problems with frequent urinary urges, which has been getting worse as well.
You are reading content posted in the Neurology Forum
Find out how beta-blocker eye drops show promising results for acute migraine relief.
In this special Missouri Medicine report, doctors examine advances in diagnosis and treatment of this devastating and costly neurodegenerative disease.
Here are 12 simple – and fun! – ways to boost your brainpower.
Discover some of the causes of dizziness and how to treat it.
Discover the common causes of headaches and how to treat headache pain.
Two of the largest studies on Alzheimer’s have yielded new clues about the disease
