กล้ามเนื้ออ่อนแรงในเด็ก อาจเป็นสัญญาณโรคกล้ามเนื้อฝ่อจากไขสันหลัง

Spinal Muscular Atrophy (SMA) is a genetic neuromuscular disease that causes progressive muscle weakness and atrophy, especially in movement, breathing, and swallowing. Early diagnosis and modern treatments such as gene therapy and disease-modifying drugs, combined with comprehensive multidisciplinary care, can significantly improve quality of life for children with SMA.

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Spinal Muscular Atrophy (SMA) in Children Recognizing Early Signs for Timely and Effective Treatment

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