3-methylcrotonyl CoA carboxylase 2 deficiency

Also Known As:

3 alpha methylcrotonyl-coa carboxylase 2 deficiency; 3 alpha methylcrotonylglycinuria 2; 3-Methylcrotonyl-CoA Carboxylase 2 Deficiency; 3-Methylcrotonylglycinuria II; MCC2 Deficiency; Methylcrotonylglycinuria type 2; Methylcrotonylglycinuria, Type II; methylcrotonoyl-CoA carboxylase 2 deficiency

Networked: 1 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Experts

1.	Chae, Jong Hee: 1 article (05/2023)
2.	Choi, Wooyong: 1 article (05/2023)
3.	Jung, Ju Yeol: 1 article (05/2023)
4.	Kang, Sanggoo: 1 article (05/2023)
5.	Kim, Man Jin: 1 article (05/2023)
6.	Kim, Soo Yeon: 1 article (05/2023)
7.	Kim, Taehyung: 1 article (05/2023)
8.	Ko, Jung Min: 1 article (05/2023)
9.	Lee, Jin Sook: 1 article (05/2023)
10.	Park, Lae-Jeong: 1 article (05/2023)

Related Diseases

1.	Propionic Acidemia 05/01/2023 - "In prospective clinical validation, 13.5% patients presented with medically actionable diseases, including short- or medium-chain acyl-CoA dehydrogenase deficiencies (N=6), hyperphenylalaninemia (N=2), mucopolysaccharidosis type IVA (N=1), alpha thalassemia (N=1), 3-methylcrotonyl-CoA carboxylase 2 deficiency (N=1), propionic acidemia (N=1), glycogen storage disease, type IX(a) (N=1), congenital myasthenic syndrome (N=1), and citrullinemia, type II (N=1). "
2.	Congenital Myasthenic Syndromes (Myasthenia Gravis, Congenital) 05/01/2023 - "In prospective clinical validation, 13.5% patients presented with medically actionable diseases, including short- or medium-chain acyl-CoA dehydrogenase deficiencies (N=6), hyperphenylalaninemia (N=2), mucopolysaccharidosis type IVA (N=1), alpha thalassemia (N=1), 3-methylcrotonyl-CoA carboxylase 2 deficiency (N=1), propionic acidemia (N=1), glycogen storage disease, type IX(a) (N=1), congenital myasthenic syndrome (N=1), and citrullinemia, type II (N=1). "
3.	Citrullinemia 05/01/2023 - "In prospective clinical validation, 13.5% patients presented with medically actionable diseases, including short- or medium-chain acyl-CoA dehydrogenase deficiencies (N=6), hyperphenylalaninemia (N=2), mucopolysaccharidosis type IVA (N=1), alpha thalassemia (N=1), 3-methylcrotonyl-CoA carboxylase 2 deficiency (N=1), propionic acidemia (N=1), glycogen storage disease, type IX(a) (N=1), congenital myasthenic syndrome (N=1), and citrullinemia, type II (N=1). "
4.	alpha-Thalassemia 05/01/2023 - "In prospective clinical validation, 13.5% patients presented with medically actionable diseases, including short- or medium-chain acyl-CoA dehydrogenase deficiencies (N=6), hyperphenylalaninemia (N=2), mucopolysaccharidosis type IVA (N=1), alpha thalassemia (N=1), 3-methylcrotonyl-CoA carboxylase 2 deficiency (N=1), propionic acidemia (N=1), glycogen storage disease, type IX(a) (N=1), congenital myasthenic syndrome (N=1), and citrullinemia, type II (N=1). "
5.	Mucopolysaccharidosis IV (Morquio Syndrome) 05/01/2023 - "In prospective clinical validation, 13.5% patients presented with medically actionable diseases, including short- or medium-chain acyl-CoA dehydrogenase deficiencies (N=6), hyperphenylalaninemia (N=2), mucopolysaccharidosis type IVA (N=1), alpha thalassemia (N=1), 3-methylcrotonyl-CoA carboxylase 2 deficiency (N=1), propionic acidemia (N=1), glycogen storage disease, type IX(a) (N=1), congenital myasthenic syndrome (N=1), and citrullinemia, type II (N=1). "

Related Drugs and Biologics

1.	Acyl-CoA Dehydrogenase (Medium-Chain Acyl-Coenzyme A Dehydrogenase)