Amino Acid Disorders 3
The Amino Acid Disorders 3 session will be discussing NKH, Lysine metab (GA1 and PDE).
This educational activity is supported by an educational grant from Ultragenyx.
- Recall how to diagnosis patients with disorders of glycine and lysine metabolism through biochemical or genetic testing.
- Describe the phenotypic heterogeneity of patients with glycine and lysine metabolism disorders.
- Summarize common treatment approaches for patients with glycine and lysine metabolism disorders.
Curtis Coughlin, MD
Children's Hospital Colorado
Planners, faculty, and others in control of content (either individually or as a group) have no relevant financial relationships with ineligible companies.
Children’s Hospital Colorado is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.
Children’s Hospital Colorado designates this Live activity for a maximum of 1.50 AMA PRA Category 1 Credit(s)™. Physicians should only claim credit commensurate with the extent of their participation in the activity.
A general certificate of attendance will be available after the completion of the online evaluation. Claim only credit commensurate of your conference attendance.
- 1.50 AMA PRA Category 1 Credit™
- 1.50 Attendance