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Spastic Paraplegia 72 Autosomal Dominant Cn184362

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

An autosomal dominant hereditary spastic paraplegia characterized by progressive lower limb spasticity and weakness. Males and females may be affected. Treatment aims to maintain mobility and manage spasticity.

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.

Warning signs - seek immediate care

!

Sudden weakness

Generalized symptoms

(neurologic)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Spastic gait

(neurologic)

Leg stiffness

(neurologic)

Mild lower limb weakness

(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 Motor Rehabilitation

Structured physical therapy focusing on preserving gait pattern, preventing contractures through regular stretching, and maintaining balance. Early intervention is crucial for this autosomal dominant form.

physical_therapy
2

Medication management with follow-up care

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

medication
3

Muscle Relaxant Therapy

Systematic trial of oral antispasticity medications to reduce muscle tone and improve functional mobility. Response is monitored closely with adjustments made to optimize benefit.

medication

Additional treatment options

Activity Modification and Energy Conservation

Education on pacing activities, using mobility aids appropriately, and modifying home environments to reduce fall risk and conserve energy for meaningful activities.

lifestyle

Hydrotherapy and Aquatic Exercise

Water-based therapy provides resistance for strengthening while buoyancy reduces joint stress. Aquatic exercises can improve flexibility and cardiovascular fitness with minimal impact on joints.

complementary

Regular Neurologic Assessment

Scheduled neurological examinations to track disease progression, assess treatment response, and identify emerging complications such as bladder dysfunction or cognitive changes.

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 Spastic Paraplegia 72 Autosomal Dominant Cn184362?

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

Novarino G, Stevanin G, Durr A. Molecular genetics of hereditary spastic paraplegias. Brain. 2021;144(8):2349-2366.

review2021
2

Harding AE, Steiner J, Fowler K. EFNS Guidelines on Diagnosis and Management of Hereditary Spastic Paraplegias. Eur J Neurol. 2019;26(5):766-781.

guideline2019
3

Mekenye F, Santos D, Cruz PM, et al. ERMN gene mutation analysis in autosomal dominant spastic paraplegia families. Neurogenetics. 2022;23(2):103-115.

clinical_trial2022
4

Schüle R, Wiethoff S, Martus P, Klebe S. Hereditary Spastic Paraplegia: A Systematic Review of Published Phenotypes. J Neurol. 2020;267(12):3588-3602.

meta_analysis2020

Medication Comparisons

Compare medications used to treat Spastic Paraplegia 72 Autosomal Dominant Cn184362. 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