Viewing Study NCT05910151

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Study NCT ID: NCT05910151

Status: UNKNOWN

Last Update Posted: 2023-06-18

First Post: 2023-06-08

Is NOT Gene Therapy: True

Has Adverse Events: False

Brief Title: Selective Screening of Children for Hereditary Metabolic Diseases by Tandem Mass Spectrometry in Kazakhstan

Sponsor: West Kazakhstan Medical University

Organization:

Overview Dates Organization Conditions Design Enrollment Locations Outcomes Modules Raw JSON

Conditions:

Condition Brief	Condition Text	View

None	Propionic/Methylmalonic Acidemias	View
None	Maple Syrup Urine Disease	View
None	Citrullinemia	View
None	Argininosuccinic Aciduria	View
None	Ornithine Transcarbamylase Deficiency	View
None	Carbamoyl Phosphate Synthetase I Deficiency	View
None	N-acetylglutamate Synthase Deficiency	View
None	Nonketotic Hyperglycinemia	View
None	Tyrosinemia	View
None	Homocystinuria	View
None	Arginase Deficiency	View
None	Isovaleric Acidemia	View
None	Short/Branched Chain Acyl-CoA Dehydrogenase Deficiency	View
None	Isobutyryl-CoA Dehydrogenase Deficiency	View
None	Glutaric Acidemia Type I	View
None	3-methylcrotonyl-CoA Carboxylase Deficiency	View
None	Biotinidase Deficiency	View
None	Malonyl-CoA Decarboxylase Deficiency	View
None	Beta-ketothiolase Deficiency	View
None	3-hydroxy-3-methylglutaryl-CoA Lyase Deficiency	View
None	3-methylglutaconyl-CoA Hydratase Deficiency	View
None	Medium-chain Acyl-CoA Dehydrogenase Deficiency	View
None	Very Long-chain Acyl-CoA Dehydrogenase Deficiency	View
None	Long-chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency	View
None	Glutaric Acidemia Type II	View
None	Primary Carnitine Deficiency	View
None	Carnitine Palmitoyltransferase I Deficiency	View
None	Carnitine Palmitoyltransferase II Deficiency	View
None	Carnitine-acylcarnitine Translocase Deficiency	View

Keywords:

Keyword Brief	Keyword Text	View

None	Inborn errors of metabolism, MS/MS, selective screening	View