Pediatic Spinal Muscular Atrophy Program | Boston Children's Hospital
The Pediatric Spinal Muscular Atrophy Program in Boston, MA is dedicated to providing comprehensive care and support for individuals with spinal muscular atrophy (SMA), a rare hereditary genetic condition that weakens muscles throughout the body due to malfunctioning nerve cells in the spinal cord and brainstem. They offer a range of clinical services, programs, and treatments tailored to the different types of SMA, from the severe Type 1 to the milder Type 4. With a team of experienced healthcare professionals and researchers, they strive to improve the lives of patients and families affected by SMA.
The program focuses on accurate diagnosis through genetic blood tests and provides personalized treatment plans to manage symptoms such as muscle weakness, limited mobility, breathing difficulties, and feeding problems. They also conduct clinical trials and engage in research to advance understanding and develop innovative therapies for SMA. Committed to health equity, the program offers resources and support services for patients and families, ensuring access to quality care and promoting a better quality of life for individuals with SMA.
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