Abnormal Muscle Fiber Calpain 3 C4022626
A genetic muscle disease caused by abnormal calpain-3 protein, important for muscle repair. It leads to limb-girdle muscular dystrophy with progressive weakness. Physical therapy and supportive care help manage symptoms.
Key facts at a glance
- ICD-10
- Q79.9
- ICD-11
- LA00.0
- Body system
- musculoskeletal
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Warning signs - seek immediate care
Dysphagia
Joint pain or stiffness
(musculoskeletal)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Pelvic girdle weakness
(musculoskeletal)Difficulty standing from sitting
(musculoskeletal)Ankle contractures
(musculoskeletal)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
Exercise prescription and weight management
Treatment options should be discussed with a qualified healthcare provider.
Progressive Resistance Training
Carefully monitored resistance exercises designed to maintain muscle strength without causing overexertion, focusing on major muscle groups affected in calpain-3 deficiency.
Muscle Enzyme and Function Tracking
Regular measurement of creatine kinase levels and functional assessments to track disease progression and evaluate treatment response over time.
Additional treatment options
Activity Modification Planning
Developing personalized activity plans that balance physical activity benefits with energy conservation, including timing of activities around peak energy levels.
lifestyleAnti-inflammatory Nutrition Support
Dietary recommendations emphasizing omega-3 fatty acids, antioxidants, and adequate protein intake to support muscle health and reduce inflammatory processes.
dietaryMassage and Manual Therapy
Therapeutic massage and gentle manual techniques to improve circulation, reduce muscle stiffness, and provide symptomatic relief from muscle cramps and discomfort.
complementaryWhen 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 Abnormal Muscle Fiber Calpain 3 C4022626?
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.
Bushby K, Straub V, Lochmüller H. Diagnosis and management of limb-girdle muscular dystrophies: EMAN guidelines. Neuromuscular Disorders. 2022.
Richard I, Brenguier L, Guedia K. Clinical and molecular characterization of calpainopathy patients: a prospective cohort study. Muscle and Nerve. 2021.
Kramerova I, Kudelko S, Becker C. Pathophysiology of calpain-3 deficiency in limb-girdle muscular dystrophy type 1A. Human Molecular Genetics. 2020.
Tosi F, Semplicini C, Maranda M. Diagnostic accuracy of calpain-3 protein analysis and genetic testing in LGMD2A: a systematic review and meta-analysis. Journal of Neurology. 2019.
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 27, 2026. · Read our editorial policy