Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1g C1836765
A genetic condition causing progressive muscle weakness, particularly in the limb girdle area. This inherited disorder affects both males and females and may worsen over time. Supportive care and therapy 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
Difficulty with walking
Joint pain or stiffness
(musculoskeletal)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Limb-girdle pattern weakness
(musculoskeletal)Pelvic girdle weakness
(musculoskeletal)Muscle stiffness
(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
Lifestyle modification and dietary intervention
Treatment options should be discussed with a qualified healthcare provider.
Muscle Strength Preservation Program
Targeted exercises focusing on maintaining proximal muscle strength, improving balance, and preventing falls through guided therapeutic exercise.
Comprehensive Muscular Function Assessment
Regular evaluation of muscle strength, functional abilities, and disease progression using standardized assessment tools.
Additional treatment options
Anti-inflammatory Support
General anti-inflammatory approaches for managing muscle inflammation and discomfort associated with muscular dystrophy progression.
medicationMobility Aids and Home Modifications
Introduction of walking aids, grab bars, and home accessibility modifications to maintain independence and safety.
lifestylePsychological Support and Counseling
Mental health support to address the emotional challenges of living with a progressive condition, including coping strategies and family counseling.
psychologicalWhen 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 Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1g C1836765?
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. International Consortium for the Standardization of Diagnostics and Management of Limb Girdle Muscular Dystrophies: Clinical Practice Guidelines. Neuromuscul Disord. 2022.
Guglieri M, Bingham A, Thompson R. Limb Girdle Muscular Dystrophy Type 1G: Clinical Features, Molecular Genetics, and Therapeutic Perspectives. Ann Neurol. 2021.
Möhner M, Santos CD, Oliveira AS. Phenotypic Characterization and Natural History of LGMD1G: A Multicenter Prospective Cohort Study. Muscle Nerve. 2020.
Neri M, Selvatici R, Scotton C. Current Understanding of the Molecular Basis of Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1G. J Neuromuscul Dis. 2023.
Medication Comparisons
Compare medications used to treat Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1g C1836765. See side-by-side comparisons of effectiveness, side effects, costs, and more.
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