No cure; management focuses on supportive care, improving quality of life
Spinal muscular atrophy is a genetic disorder affecting the motor neurons in the spinal cord, leading to muscle weakness. Treatment may include supportive care, medications, and, in some cases, gene therapy. Regular monitoring is important for assessing disease progression, managing symptoms, and adjusting interventions as needed.
Genetic disorder causing progressive muscle weakness
Muscle weakness, atrophy, difficulty breathing
Genetic testing, clinical evaluation
Variable, depends on the type and progression of SMA
Muscle weakness, complications affecting mobility
Genetic mutations (SMN1 gene)
Supportive care, physical therapy, respiratory support
Supportive care, physical therapy, respiratory support
Genetic disorder affecting motor neurons
Supportive care, physical therapy, sometimes medication
For personalized advice and care, always seek the assistance of healthcare professionals. This information is meant for general understanding and not as a replacement for professional medical advice.
Share: