Outcomes of cases with 3-methylcrotonyl-CoA carboxylase (3-MCC) deficiency - Report from the Inborn Errors of Metabolism Information System

Keyphrases

• Inborn Errors of Metabolism 100%
• Newborn Screening 100%
• Developmental Abnormality 100%
• 3-methylcrotonyl-CoA Carboxylase Deficiency 100%
• C5OH 50%
• Children at Risk 25%
• Metabolic 25%
• Developmental Disabilities 25%
• Methyl 25%
• Later Life 25%
• Hyperammonemia 25%
• Biochemical Markers 25%
• Inborn Errors 25%
• Predictive Marker 25%
• Metabolic Abnormalities 25%
• Acidosis 25%
• Lactic Acidosis 25%
• Biochemical Abnormalities 25%
• Expanded Newborn Screening 25%
• Ascertainment Bias 25%
• Leucine Metabolism 25%
• 3-Methylcrotonyl-CoA Carboxylase 25%
• Crotonyl-CoA 25%
• Metabolic Symptoms 25%
• Normal Prior 25%
• Carboxylase Deficiency 25%
• System Database 25%

Medicine and Dentistry

• Newborn Screening 100%
• Inborn Error of Metabolism 100%
• Carboxylase 100%
• Methylcrotonyl-CoA 100%
• Developmental Abnormality 60%
• Developmental Disorder 20%
• Neonatal Infant 20%
• Hyperammonemia 20%
• Retrospective Study 20%
• Acidosis 20%
• Leucine 20%
• Predictive Marker 20%
• Lactic Acidosis 20%
• Biochemical Marker 20%
• Ascertainment Bias 20%
• Crotonyl-CoA 20%
• Children at Risk 20%

Pharmacology, Toxicology and Pharmaceutical Science

• Carboxylase 100%
• Methylcrotonyl-CoA 100%
• Inborn Error of Metabolism 100%
• Retrospective Study 33%
• Leucine 33%
• Biochemical Marker 33%
• Crotonyl-CoA 33%
• Lactic Acidosis 33%
• Hyperammonemia 33%
• Developmental Disorder 33%