Carbohydrate-deficient glycoprotein syndrome type Ib.
What does CDG stand for?
CDG stands for Carbohydrate-Deficient Glycoprotein
This definition appears frequently and is found in the following Acronym Finder categories:
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See other definitions of CDG
We have 152 other meanings of CDG in our Acronym Attic
- Caloric-Deprivation Failure To Thrive
- Communication for Development Foundation Uganda
- Cordova District Fishermen United (Cordova, AK)
- Centre for Domestic and Family Violence Research (Central Queensland University; Australia)
- California Department of Fish and Wildlife
- Cloud-Delivered Firewall (Cisco Umbrella cloud security platform)
- Contemporary Dance Fort Worth (Texas)
- Council for Drug Free Youth (Jefferson City, MO)
- Caisse de Dépôt et de Gestion (French; Moroccan federal depository)
- Capacitance Diaphragm Gauge
- Career Development Grant (various organizations)
- Carl Duisberg Gesellschaft eV
- Casting Directors' Guild (cinema)
- Cave Diving Group (UK)
- CDMA Development Group
- Center for Digital Government (Folsom, CA)
- Centre de Gestion
- Centre des Droits des Gens (French: Centre for People’s Rights; Morocco)
- Centre Downwash Generating (aerodynamics, fluid dynamics, automotive)
- Centre for Democratic Governance (various locations)
Samples in periodicals archive:
Q Our 3-year-old daughter was recently diagnosed with carbohydrate-deficient glycoprotein syndrome.
Carbohydrate-deficient glycoprotein syndrome: clinical expression in adults with a new metabolic disease.
Congenital disorders of glycosylation (CDG), formerly named carbohydrate-deficient glycoprotein syndrome, are rare hereditary disorders caused by mutations in the genes coding for enzymes involved in the biosynthesis of glycoproteins and other glycoconjugates (1).
Abnormal synthesis of dolichol-linked oligosaccharides in carbohydrate-deficient glycoprotein syndrome.
The isoform profile is changed in several pathologic conditions not related to alcohol, particularly the carbohydrate-deficient glycoprotein syndrome (15).
Capillary electrophoresis-based separation of transferrin sialoforms in patients with carbohydrate-deficient glycoprotein syndrome.
Phosphomannomutase deficiency is a cause of carbohydrate-deficient glycoprotein syndrome type I.