Muscular Pathologies
Specialized Care for Neuromuscular & Muscle Weakness Disorders
Overview
We diagnose and manage genetic and acquired muscle disorders in children, including Duchenne Muscular Dystrophy (DMD), spinal muscular atrophy, and inflammatory myopathies.
Our team works closely with physical therapists to design stretching programs that prevent joint contractures.
Common Symptoms & Indications
- ✕ Difficulty climbing stairs
- ✕ Calf muscle enlargement (pseudohypertrophy)
- ✕ Frequent falls or waddling gait
- ✕ Inability to stand up from the floor without support
Clinical Procedure & Diagnostics
Clinical assessment of muscle strength (e.g., Gowers' sign), NCV/EMG testing, serum CK level analysis, and coordination of genetic tests (MLPA/NGS).
Key Recovery Benefits
- ✓ Early diagnosis and initiation of modern disease-modifying therapies
- ✓ Joint contracture prevention
- ✓ Maintained walking mobility
- ✓ Supportive care coordination
Rehabilitation & Recovery Timeline
Clinical Workup
Strength testing, Gowers' sign check, and initial lab tests.
Diagnostics
EMG/NCV and genetic testing for definitive diagnosis.
Supportive Care
Physiotherapy, orthotic splints, and medical management.
Frequently Asked Questions
DMD is a genetic muscle disease that causes progressive muscle weakness, typically starting in early childhood and primarily affecting boys.
Diagnosis is made using blood tests (creatine kinase), EMG/NCV studies, and is confirmed using genetic blood tests or a muscle biopsy.
Yes, modern treatments like gene therapies, exon-skipping drugs, and steroids help slow disease progression and maintain mobility longer.
It keeps muscles flexible, prevents joint contractures, preserves respiratory strength, and helps children maintain walking ability for a longer period.
Consult Specialist
Schedule a detailed clinical assessment with Dr. Amodini Walia at The Ved Clinic Dehradun.
Request Appointment