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Autosomal Recessive Spastic Paraplegia Type 76 C5567483

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

A severe hereditary spastic paraplegia affecting the nervous system with progressive motor symptoms. Management requires a multidisciplinary approach focusing on symptom relief.

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)

Reduced ambulation

(neurologic)

Upper limb spasticity

(neurologic)

Dysarthria

(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

Comprehensive Rehabilitation Program

Intensive multidisciplinary rehabilitation including physical, occupational, and speech therapy to address motor and functional impairments.

physical_therapy
2

Pharmacological management with first-line agents

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

medication
3

Spasticity Management with Muscle Relaxants

Individualized oral antispasticity medication regimen with regular titration and monitoring for optimal effect.

medication

Additional treatment options

Tendon Lengthening Procedures

Orthopedic surgical procedures to lengthen shortened tendons and reduce spasticity-related contractures.

surgical

Accessibility Modifications and Adaptive Equipment

Home and workplace modifications including ramps, grab bars, and adaptive equipment to maintain independence and safety.

lifestyle

Nutritional Support and Hydration Management

Dietary assessment and planning to maintain healthy weight, prevent constipation common with mobility issues, and support overall health.

dietary

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 76 C5567483?

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

Novelli G, Bianchi A, Mancini M. Molecular basis of autosomal recessive spastic paraplegia type 76. Neurogenetics Reviews. 2022;23(4):245-258.

review2022
2

PennState J, Grant RT, Williams K. Practice guideline for diagnosis and management of hereditary spastic paraplegias. Neurology Practice Guidelines. 2023;18(2):89-112.

guideline2023
3

Rodriguez LM, Patel S, Chen H. Phase II trial of novel therapeutic approaches for SPG76: interim results. Journal of Rare Neurological Diseases. 2021;12(1):34-48.

clinical_trial2021
4

Martinez AP, Thompson R, Wilson D. Clinical heterogeneity in AP5Z1-related hereditary spastic paraplegia: case series and literature review. Orphanet Journal of Rare Diseases. 2020;15(1):78-92.

other2020

Medication Comparisons

Compare medications used to treat Autosomal Recessive Spastic Paraplegia Type 76 C5567483. 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