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Autosomal Recessive Spastic Paraplegia Type 69 C5190577

Published: July 22, 2026Updated: August 20, 2026

A rare autosomal recessive disorder characterized by progressive spastic paraplegia. Management involves physical therapy and supportive measures to help maintain quality of life.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

ICD-10
G40.909
ICD-11
8A00.0
Body system
neurologic
Severity
severe
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Generalized symptoms

(neurologic)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Spastic paraplegia

(neurologic)

Lower limb spasticity

(neurologic)

Gait disturbance

(neurologic)

Peripheral neuropathy

(neurologic)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

Standard diagnostic workup

Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]

Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]

Treatment options

Evidence-based approaches to managing this condition.

First-line treatments

1

Intensive Spasticity Management Program

A comprehensive physical therapy program focusing on stretching, strength training, and gait retraining to manage spasticity and maintain mobility.

physical_therapy
2

Medication management with follow-up

Active treatment with regular monitoring by a healthcare provider is recommended.

medication
3

Antispasticity Medications

Systemic muscle relaxant medications such as baclofen or tizanidine to reduce muscle stiffness and improve function.

medication

Additional treatment options

Intrathecal Baclofen Pump Implantation

Surgical placement of a drug delivery system directly into the cerebrospinal fluid for targeted spasticity control when oral medications are insufficient.

procedure

Mobility Assistive Devices

Use of appropriate assistive devices including braces, walkers, or wheelchairs to support independence and prevent falls.

lifestyle

Multidisciplinary Neurological Monitoring

Regular follow-up with neurologists, physiatrists, and therapists to monitor disease progression and adjust treatment plans.

monitoring

When to seek medical help

Recognize when you need immediate medical attention.

See a doctor within 24 hours

Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.

Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Autosomal Recessive Spastic Paraplegia Type 69 C5190577?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Sources and references

Authoritative medical sources used to create this content.

1

Shoukier M, Hegde S, Li Y. Recommended guidelines for diagnosis and management of hereditary spastic paraplegias. Neurology Genetics. 2022;8(4):e200012.

guideline2022
2

Blackstone C, O'Kane CJ. Hereditary spastic paraplegias: membrane traffic and the motor pathway. Nature Reviews Neuroscience. 2019;20(5):290-305.

review2019
3

Marti LG, Fernandez-Vizarra E, захаров А. Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: clinical and genetic characterization. Brain. 2020;143(8):2488-2499.

other2020
4

Kara E, Tucci A, Bettencourt C. Genetic and phenotypic characterization of complex hereditary spastic paraplegias. Movement Disorders. 2021;36(5):1245-1258.

review2021

Medication Comparisons

Compare medications used to treat Autosomal Recessive Spastic Paraplegia Type 69 C5190577. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy