congenital muscular dystrophy

Public Health Genomics Knowledge Base (v1.2)

From Guideline Database

This database contains updated guidelines, policies and recommendations on genomic research and practice, as provided by professional organizations, federal advisory groups, expert panels and policy groups.

---

• Evidence-based guideline summary: Evaluation, diagnosis, and management of congenital muscular dystrophy: Report of the Guideline Development Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic Medicine.
  Published 2015 (American Academy of Neurology - Guideline Development Subcommittee) (American Association of Neuromuscular & Electrodiagnostic Medicine - Practice Issues Review Panel)
• Evidence-based guideline summary: Evaluation, diagnosis, and management of facioscapulohumeral muscular dystrophy: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic Medicine.
  Published 2015 (American Academy of Neurology - Guideline Development, Dissemination, and Implementation Subcommittee) (American Association of Neuromuscular & Electrodiagnostic Medicine - Practice Issues Review Panel)
• Evidence-based guideline summary: diagnosis and treatment of limb-girdle and distal dystrophies: report of the guideline development subcommittee of the American Academy of Neurology and the practice issues review panel of the American Association of Neuromuscular & Electrodiagnostic Medicine.
  Published 2014 (Guideline Development Subcommittee of the American Academy of Neurology) (Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic Medicine)

more