American College Medical Genetics (ACMG)
March 23-26, 2006  San Diego, California

Recognition, Diagnosis and Treatment of Pediatric Neurotransmitter Disorders
Moderator: K. Michael Gibson, PhD, FACMG,
University of Pittsburgh School of Medicine, Pittsburgh, PA

Cerebrospinal Fluid: A Critical Component for the Diagnosis of Pediatric Neurotransmitter Disorders
Keith Hyland, PhD,
Horizon Medicine, Atlanta, GA

Clinical Features of Tyrosine Hydroxylase Deficiency, Aromatic Amino Acid Decarboxylase Deficiency, and Autosomal Dominant GTP-Cyclohydrolase Deficiency (Segawa Disease)
Kathryn J. Swoboda, MD, FACMG,
University of Utah School of Medicine, Salt Lake City, UT

Heritable Succinate Semialdehyde Dehydrogenase Deficiency, a Disorder of GABA Catabolism
Phillip Pearl, MD,
George Washington University School of Medicine  and
Children's National Medical Center, Washington, DC