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Spinal Muscular Atrophy (SMA) Care Center

SMA Team

The University of Rochester SMA Care Center mission is to provide most up to date multidisciplinary care to patients with SMA of all ages and at all stages of disease, including newborns diagnosed through the New York State Newborn Screening Program. Our goal is to make a positive impact on the quality of life of infants, children, adolescents and adults affected by SMA by providing a team of experts in all specialties needed to best care for SMA, a friendly and supportive atmosphere, and a coordinated care that is highly accessible for families. We focus on all aspects of disease including:

  • A timely diagnosis with genetic confirmation and genetic and family counseling
  • Treatment with all currently FDA approved drugs for SMA (Spinraza, Evrysdi and Zolgensma)
  • Prevention and management of secondary symptoms and complications, including respiratory, nutrition, and bone health
  • Access to clinical trials
  • Coordination of care with schools and other providers.

Our specialized SMA team include Neuromuscular Neurologists, Pulmonologists (pediatric and adult), Physical Therapists, Nurses, Nurse Practitioners, genetic counselor, social worker, orthopedic surgeons (pediatric and adult), nutritionist/GI, clinic coordinator, specialty pharmacy.

For additional SMA information and patient resources, see: CureSMA.

Welcome from the Director

CiafoloniWelcome to the University of Rochester Spinal Muscular Atrophy (SMA) Clinic. Our mission is to provide cutting edge, patient-centered, multidisciplinary care of the highest quality to patients of all ages leaving with SMA; to conduct innovative basic and translational research and provide access to cutting edge clinical trials; to provide timely and coordinated access to newly approved drugs for SMA, including gene therapy and gene-based drugs. We serve our community and welcome patients from other regions and are willing to work with our patient’s local physicians. Our team has decades of experience in caring for SMA patients and their families and includes expert neuromuscular neurologists, genetic counselors, nurses and nurse practitioners, physical therapists, pediatric and adult cardiologists and pulmonologists, and palliative care physicians. We have a longstanding partnership with the Muscular Dystrophy Association (MDA) and CureSMA. We welcome you to browse our website to learn more about our clinical programs and our research enterprise.

Emma Ciafaloni, M.D., FAAN, FANA, Director

 

Request an Appointment

Call: (585) 275-2559

Fax a Referral: (585) 784-7919