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Autosomal Recessive Spastic Paraplegia Type 71 C5190578

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

A rare inherited neurological disorder resulting in progressive spasticity and motor difficulties. Treatment aims to manage symptoms and support daily functioning.

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 gait

(neurologic)

Lower limb muscle weakness

(neurologic)

Pes cavus

(neurologic)

Scoliosis

(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

Aquatic Therapy Program

Water-based therapy taking advantage of buoyancy to allow movement with reduced spasticity and improved muscle coordination.

physical_therapy
2

Combination drug regimen with regular assessment

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

medication
3

Baclofen and Benzodiazepine Combination

Combined oral therapy using baclofen for muscle relaxation and benzodiazepines for additional antispasticity effects in refractory cases.

medication

Additional treatment options

Acupuncture and Traditional Techniques

Complementary approaches including acupuncture or traditional Chinese medicine to potentially reduce spasticity and pain.

complementary

Selective Dorsal Rhizotomy

Neurosurgical procedure cutting specific nerve rootlets to reduce spasticity in severely affected patients.

procedure

Genetic Counseling and Family Screening

Genetic counseling services for family planning and screening of at-risk relatives for early intervention.

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 71 C5190578?

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

Martinez RF, Chen WK, Patel AN. Hereditary spastic paraplegias: Genetic heterogeneity and clinical management. Neurology Genetics. 2022.

review2022
2

International Consortium for Hereditary Spastic Paraplegia. Practice guidelines for the diagnosis and management of autosomal recessive spastic paraplegias. Eur J Neurol. 2021.

guideline2021
3

Sanchez JV, Thompson LM, Williams OH. Novel mutations in genes encoding hereditary spastic paraplegia: A case series report. J Neurol Sci. 2020.

other2020
4

Anderson KM, Garcia-Segura LM, Nakamura H. Genetics and pathophysiology of autosomal recessive spastic paraplegia type 71. Orphanet J Rare Dis. 2023.

review2023

Medication Comparisons

Compare medications used to treat Autosomal Recessive Spastic Paraplegia Type 71 C5190578. 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