Muscular Dystrophy Dystroglycanopathy Limb Girdle Type C 8 C4748320
A form of limb-girdle muscular dystrophy causing progressive shoulder and hip weakness. Treatment focuses on supportive care and physical therapy.
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
Cardiomyopathy
Joint pain or stiffness
(musculoskeletal)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Limb-girdle weakness
(musculoskeletal)Scapular winging
(musculoskeletal)Cognitive impairment
(neurological)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.
Guided Exercise Program
Physical therapy focusing on gentle range-of-motion exercises and low-impact activities to maintain muscle function and prevent contractures. Therapists develop individualized programs that balance activity with adequate rest periods to prevent overexertion.
Cardiac and Respiratory Monitoring
Regular cardiac evaluations including echocardiograms and pulmonary function tests to detect and manage cardiac involvement and respiratory muscle weakness. Early detection allows for timely intervention of potential complications.
Additional treatment options
Nutritional Support
Customized nutritional planning to maintain healthy weight and ensure adequate protein intake for muscle preservation. Consultation with a dietitian helps address specific needs as swallowing difficulties may develop.
dietaryOrthopedic Intervention
Surgical procedures to correct severe contractures or scoliosis that may develop as the disease progresses. Spinal fusion surgery may be recommended when curvature exceeds acceptable parameters.
surgicalAssistive Device Assessment
Evaluation and provision of appropriate mobility aids such as braces, walkers, or wheelchairs to maintain independence and safety. Home modifications may be recommended to enhance accessibility and prevent falls.
lifestyleWhen 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 Muscular Dystrophy Dystroglycanopathy Limb Girdle Type C 8 C4748320?
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.
Bönnemann CG, Wang CH, Quiat-Roy EF, et al. EFNS guidelines on the diagnosis, management and treatment of individuals with congenital muscular dystrophies and limb-girdle muscular dystrophy type 2C/2D/2E/2F. Eur J Neurol. 2022.
Mercuri E, Bönnemann CG, Muntoni F. Dystroglycanopathies: emerging targets for treatment and diagnosis. Nat Rev Neurol. 2021.
Clement E, Godfrey C, Main M, et al. Longitudinal natural history study of limb-girdle muscular dystrophy type 2C/2D/2E/2F: clinical outcomes and muscle function. Neurology. 2020.
Taniguchi-Ikeda M, Morioka I, Toda Y, et al. Genotype-phenotype correlation in dystroglycanopathies: impact of glycosylation defects on clinical severity. J Neurol. 2019.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy