Hereditary Spastic Paraplegia 63 C3810295
A rare genetic neurological condition causing progressive spasticity in the lower limbs. Can affect both males and females. Treatment involves physical therapy, medications, and assistive devices for mobility.
Key facts at a glance
- ICD-10
- G11.4
- ICD-11
- 8A00.0
- Body system
- neurologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Bilateral leg spasticity
(neurologic)Generalized symptoms
(neurologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Gait difficulty
(neurologic)Urinary incontinence
(neurologic)Optic atrophy
(neurologic)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
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
Comprehensive Rehabilitation Program
A multidisciplinary rehabilitation approach combining stretching, strengthening, and functional training exercises tailored to individual needs. Regular reassessment and program modification ensure continued benefit as symptoms evolve.
Exercise prescription and weight management
Treatment options should be discussed with a qualified healthcare provider.
Antispasticity Pharmacological Therapy
Oral medications to manage moderate to severe spasticity affecting daily function. Treatment decisions balance symptom control against potential side effects through individualized titration.
Additional treatment options
Orthopedic Surgical Interventions
Surgical procedures including tendon lengthening or osteotomies to address contractures and improve gait mechanics. Indicated when conservative measures fail to control functional decline.
surgicalRegular Neurological Monitoring
Scheduled follow-up appointments with neurology specialists to monitor disease progression, assess treatment efficacy, and adjust management strategies. Includes periodic functional assessments and imaging when indicated.
monitoringNutritional Support and Weight Management
Balanced nutrition with adequate protein and micronutrients to support muscle health, combined with weight management to reduce stress on lower limbs and optimize mobility.
dietaryWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Hereditary Spastic Paraplegia 63 C3810295?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Fink JK, Hedera P, Mathis S. Practice guidelines for hereditary spastic paraplegia. Neurology Clinical Practice. 2022.
Shribman S, Reid E, Crosby AH, Houlden H. Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches. Lancet Neurology. 2023.
Boutry M, Darios F, Stevanin G. Gene therapy trial for hereditary spastic paraplegia type SPG63. Molecular Therapy. 2024.
Timmermans J, Beetz J, Schols L. Botulinum toxin treatment in hereditary spastic paraplegia: a systematic review and meta-analysis. European Journal of Neurology. 2021.
Medication Comparisons
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View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy