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Department of Health and Human Services
Advisory Committee on Heritable Disorders in Newborns and Children
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Twenty-Eighth Meeting of the Secretary’s Advisory Committee on Heritable Disorders in Newborns and Children

September 13-14, 2012


Newborn Screening Case Definitions and Quality Indicators (PDF - 511 KB)
Jelili Ojodu, MPH

Final Condition Review Matrix (PDF - 479 KB)
Alex Kemper, MD, MPH, MS

Adrenoleukodystrophy: Nomination and Prioritization Report (PDF - 1,149 KB)
Fred Lorey, PhD

Pompe Disease: Condition Review Update (PDF - 442 KB)
Alex Kemper, MD, MPH, MS

Ethical, Legal, and Social Implications Program (PDF - 5,596 KB)
Jean McEwen, JD, PhD

Lab Standards and Procedures Subcommittee Report (PDF - 760 KB)
Fred Lorey, PhD

Education and Training Subcommittee Report (PDF - 106 KB)
Beth Tarini, MD, MS, FAAP

Follow-up and Treatment Subcommittee Report (PDF - 330 KB)
Carol Greene, MD

Multistate Analysis of Single or Routine Second Testing for Hypothyroidism and CAH (PDF - 1,333 KB)
Stuart Shapira, MD, PhD

CDC Recommendations for GLP in Biochemical Genetic Testing and NBS for Inherited Metabolic Disorders (PDF - 471 KB)
Bin Chen, PhD, FACMG

Pregnancy and Health Profile: Prenatal Family History Project (PDF - 976 KB)
Joan Scott, MS, CGC

Population-based Carrier Screening Work Group Interim Report (PDF - 246 KB)
Meredith Weaver, PhD, ScM, CGC

IOM Meeting Summary: Economics of Genomic Medicine (PDF - 446 KB)
Catherine Wicklund, MS, CGC