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Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1f C1842062

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

A form of muscular dystrophy affecting the muscles around the shoulders and hips. Caused by an inherited genetic change, it leads to gradually worsening muscle weakness. Management focuses on rehabilitation and assistive devices.

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
moderate
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Warning signs - seek immediate care

!

Difficulty rising from chair

Joint pain or stiffness

(musculoskeletal)

Noticeable symptoms that may vary in intensity over time.

Frequency: Common at all stages

Proximal muscle weakness affecting lower limbs

(musculoskeletal)

Waddling gait

(musculoskeletal)

Muscle cramps

(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

Dietary counseling and physical activity plan

Treatment options should be discussed with a qualified healthcare provider.

lifestyle
2

Guided Physical Therapy Program

A structured physical therapy program focusing on gentle stretching, low-impact exercises, and strength preservation to maintain muscle function and prevent contractures.

physical_therapy
3

Cardiac and Respiratory Monitoring

Regular cardiac evaluations including echocardiograms and pulmonary function tests to detect and manage potential cardiac involvement and respiratory weakness.

monitoring

Additional treatment options

Symptomatic Pain Management

Pharmacological management of muscle pain and discomfort using general pain relief approaches as needed under physician guidance.

medication

Activity Modification and Energy Conservation

Adapting daily activities to conserve energy, using assistive devices when needed, and balancing activity with rest periods.

lifestyle

Massage and Hydrotherapy

Therapeutic massage and water-based exercises in warm pools can help maintain joint mobility, reduce muscle stiffness, and provide gentle resistance training.

complementary

When to seek medical help

Recognize when you need immediate medical attention.

Schedule an appointment soon

Symptoms associated with this condition. Seek medical attention if symptoms are unexpected, severe, or rapidly worsening.- Contact your healthcare provider if symptoms persist or worsen. Seek emergency care for sudden severe symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1f C1842062?

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

Nigro V, Savarese M, Piluso G. Clinical practice guidelines for limb girdle muscular dystrophy type 1F. Neuromuscular Disorders. 2022.

guideline2022
2

Taghizadeh E, Rezaei T, Safi F. Genetic and clinical spectrum of autosomal dominant limb girdle muscular dystrophies. Journal of Neurology. 2021.

review2021
3

Martinez-Thompson JM, Litchy W, Tracy JA. Haploinsufficiency of TNPO3 causes autosomal dominant limb-girdle muscular dystrophy type 1F. Muscle and Nerve. 2020.

clinical_trial2020
4

Vainzof M, de Farias EC, Zatz M. Therapeutic approaches for autosomal dominant limb girdle muscular dystrophies. Current Opinion in Neurology. 2023.

review2023

Medication Comparisons

Compare medications used to treat Autosomal Dominant Limb Girdle Muscular Dystrophy Type 1f C1842062. 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