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Autosomal Recessive Limb Girdle Muscular Dystrophy Type 2k C1836373

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

A genetic disorder causing progressive muscle weakness in the shoulders and hips. Symptoms usually begin in childhood. Treatment involves therapy and supportive measures.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

ICD-10
Q79.9
ICD-11
LA00.0
Body system
musculoskeletal
Severity
severe
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Joint pain or stiffness

(musculoskeletal)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Proximal muscle weakness

(musculoskeletal)

Difficulty climbing stairs

(musculoskeletal)

Calf pseudohypertrophy

(musculoskeletal)

Scapular winging

(musculoskeletal)

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

Pharmacological management with first-line agents

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

medication
2

Stretching and contracture prevention program

Daily stretching routines and positioning programs specifically designed to prevent or delay contractures, particularly in hip flexors and ankle plantar flexors.

physical_therapy
3

Multidisciplinary disease surveillance

Coordinated monitoring across cardiology, pulmonology, and physiatry to comprehensively track disease progression and intervene appropriately.

monitoring

Additional treatment options

Spinal scoliosis management

Surgical spinal fusion may be necessary when scoliosis develops to improve sitting balance, respiratory function, and comfort in wheelchair-dependent patients.

surgical

Massage and soft tissue therapy

Therapeutic massage to improve circulation, reduce muscle stiffness, and provide symptomatic relief from chronic muscle tightness and discomfort.

complementary

Family-centered support services

Comprehensive psychosocial support addressing the family unit, including siblings and caregivers, to build resilience and coping strategies.

psychological

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 Autosomal Recessive Limb Girdle Muscular Dystrophy Type 2k C1836373?

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

Böhm J, Gundesli H. European consensus guidelines on management of limb girdle muscular dystrophies. Neuromuscul Disord. 2022.

guideline2022
2

Wheeler MT, Nguyen R. POMT1-related muscular dystrophy: clinical and molecular features. Curr Opin Neurol. 2021.

review2021
3

Castiglioni C, Bertini E. AAV-mediated gene therapy for LGMD2K: phase I/II clinical trial results. Mol Ther. 2023.

clinical_trial2023
4

Palmio J, Udd B. Diagnostic challenges in limb girdle muscular dystrophy type 2K. J Neurol. 2020.

review2020

Medication Comparisons

Compare medications used to treat Autosomal Recessive Limb Girdle Muscular Dystrophy Type 2k C1836373. 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