6TH ANNUAL Sanford Rare DiseaseSymposium

Discover. InspIre. Grow.

Feb. 26, 2016Sanford CenterSioux Falls, SD

Location: sanford center2301 e. 60th street N.sioux Falls, sD 57104

Please park in the south lot and enter the building at the southeast door (near the globe). see map below for directions.

credits: Sanford Health is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians. Sanford Health designates this live activity for a maximum of 6.0 AMA PRA Category I Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.

This event has been submitted to the National Society of Genetic Counselors (NSGC) for approval of Category 1 CEUs. The American Board of Genetic Counseling (ABGC) accepts CEUs approved by NSGC for purposes of recertifi cation. Approval for the requested CEUs and Contact Hours is currently pending.

Sanford Health Center for Learning is an approved provider of continuing nursing education by the Washington State Nurses Association Continuing Education Approval & Recognition Program (CEARP), an accredited approver by the American Nurses Credentialing Center’s Commission on Accreditation.

6.25 ANCC Contact Hour

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Sanford Center2301 East 60th Street,Sioux Falls, SD 57104

Sanford Center2301 East 60th StreetSioux Falls, SD 57104

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Discover. InspIre. Grow.

Agenda: 8:30 a.m. event registration/Breakfast

8:45 a.m. Welcome Address – David Pearce, PhD President, sanford research sanford Health senior scientist, children’s Health research center Professor, Department of Pediatrics, University of south Dakota sanford school of Medicine

9 a.m. What the Patient Family-Physician-Partnership Can Accomplish for Rare Genetic Disorders: the Example of Lowe Syndrome – Robert Nussbaum, MD chief Medical officer, invitae corporation

10 a.m. Assessing Gene Therapy Approached for NPC1 Disease – William Pavan, PhD Director, NHGri intramural Training office

11 a.m. Break

11:15 a.m. Complex Structural Variation in Human Genomic Disorders – Claudia Carvalho, PhD Assistant Professor, Baylor college of Medicine

12:15 p.m. Lunch

1:15 p.m. The Nuclear Envelope and Rare Disease – Howard Worman, MD Professor of Medicine and Pathology and cell Biology, college of Physicians and surgeons, columbia University

2:15 p.m. Rare Genetic Obesity Disorders: Insights for Energy Balance in the General Population – Joan Han, MD Director, Pediatric obesity Program, Le Bonheur children’s Hospital Associate Professor, Division of Pediatric endocrinology, Department of Pediatrics, University of Tennessee Health science center

3:15 p.m. Break

3:30 p.m. Translation of Gene Therapeutics in Neuromuscular Disease – Brian Kaspar, PhD Associate Professor, Nationwide children’s Hospital, ohio state University

4:30 p.m. closing remarks

About the symposium: You’re invited to the sixth Annual sanford rare Disease symposium, an event organized by the coordination of rare Diseases at sanford (corDs) and sanford children’s Health research center in honor of Global rare Disease Day

Friday, Feb. 26, 2016

registration: No cost to attend. Pre-registration required by Feb. 19, 2016.

register online at sanfordresearch.org Keyword: rare Disease symposium

Questions? email cords@sanfordhealth.org or call (877) 658-9192.