Hereditary spastic paraplegia

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What is hereditary spastic paraplegia?

Hereditary Spastic Paraplegia is not a single disease but a group of genetic disorders in which the main feature is progressive spasticity in the lower limbs due to pyramidal tract dysfunction. Onset can be at any age, from the first year of life to old age, depending on the specific genetic form.

Common symptoms reported by people with hereditary spastic paraplegia

Common symptoms
How bad it is
What people are taking for it

Reports may be affected by other conditions and/or medication side effects. We ask about general symptoms (anxious mood, depressed mood, fatigue, pain, and stress) regardless of condition.
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Treatments taken by people for hereditary spastic paraplegia

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Compare treatments taken by people with hereditary spastic paraplegia

Let’s build this page together! When you share what it’s like to have hereditary spastic paraplegia through your profile, those stories and data appear here too.

Got a question about living with hereditary spastic paraplegia? Members in the forum might have the answers.

Who has hereditary spastic paraplegia on PatientsLikeMe?

  • 0 new patients joined this month
  • 227 say hereditary spastic paraplegia is their primary condition

Age
Age Proportion # of patients
<20 0
20s 10
30s 17
40s 18
50s 17
60s 10
70+ 42
Age at first symptom
Age at first symptom Proportion # of patients
0-19 years 7
20-29 years 4
30-39 years 6
40-49 years 6
50-59 years 9
60-69 years 3
70+ years 2

Distribution of sex

Sex
Sex Proportion # of patients
Male 96
Female 148

Diagnosis status
Diagnosis status Proportion # of patients
Diagnosed 97
Not Diagnosed 13

These charts show data from hereditary spastic paraplegia patients who have completed their condition history
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