Hereditary spastic paraplegia

Hereditary spastic paraplegia is a general term for a group of rare inherited disorders that cause weakness and stiffness in the leg muscles. Symptoms gradually get worse over time.

It's also known as familial spastic paraparesis or Strümpell-Lorrain syndrome.

It's difficult to know exactly how many people have hereditary spastic paraplegia because it's often misdiagnosed.

Symptoms of hereditary spastic paraplegia

The severity and progression of symptoms will vary from person to person.

About 90% of people with hereditary spastic paraplegia have what's known as a "pure form" of the condition.

This means their symptoms are mainly confined to lower limb weakness and involuntary spasms and muscle stiffness (spasticity).

The remaining 10% have a complicated or complex form of the condition.

This means they have other symptoms in addition to the muscle weakness and spasticity.

They may have a wide range of symptoms.

Pure hereditary spastic paraplegia

The main symptoms of pure hereditary spastic paraplegia are:

People with the condition may develop leg stiffness and problems walking, such as stumbling and tripping, particularly on uneven ground.

These problems are caused by weak hip muscles and difficulty bending the foot upwards.

Some people may eventually need to use a walking aid or a wheelchair to help them get around.

Others may not need to use any type of mobility equipment.

Complicated hereditary spastic paraplegia

In complicated hereditary spastic paraplegia, additional symptoms may include:

What causes hereditary spastic paraplegia?

Most people with pure hereditary spastic paraplegia will have inherited a faulty gene from 1 of their parents.

People with the complicated form of the condition will have usually inherited a faulty gene from both parents.

The gene abnormality causes the long nerves in the spine to deteriorate.

These nerves normally control muscle tone and movement in the lower body.

Diagnosing hereditary spastic paraplegia

Hereditary spastic paraplegia is diagnosed after a thorough clinical examination and the identification of typical symptoms.

Other conditions that cause mobility problems and muscle stiffness and weakness, such as multiple sclerosis and cerebral palsy, need to be ruled out first.

A number of specialised tests may be used during diagnosis, including MRI scans of the brain and spine and cerebrospinal fluid analysis. 

In some cases, genetic testing may also be needed.

Treating hereditary spastic paraplegia

It's not possible to prevent, slow or reverse hereditary spastic paraplegia, but some of the symptoms can be managed so day-to-day activities become easier.

For example:

Complications of hereditary spastic paraplegia

Possible complications of hereditary spastic paraplegia include:


The outlook for people with hereditary spastic paraplegia varies.

Some people are severely affected and need a wheelchair, while others have mild symptoms and do not need to use a mobility aid.

Pure hereditary spastic paraplegia does not usually affect life expectancy, and most people are able to lead relatively independent and active lives.

The outlook for complicated hereditary spastic paraplegia varies between people, depending on the symptoms.

National Congenital Anomaly and Rare Disease Registration Service

If you or your child have hereditary spastic paraplegia, your clinical team may pass information about you or your child on to the National Congenital Anomaly and Rare Disease Registration Service (NCARDRS).

The NCARDRS helps scientists identify more effective ways of treating or preventing rare conditions.

You can opt out of the register at any time.

Page last reviewed: 14 February 2023
Next review due: 14 February 2026