×
About 4 results

ALLMedicine™ Alg6-cdg (cdg-ic) Center

Research & Reviews  2 results

ALG6-CDG (CDG-Ic)
https://rarediseases.info.nih.gov/diseases/9829/alg6-cdg-cdg-ic

Jun 30th, 2016 - The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs. Orpha Number: 79320 Definition A form of congenital disorders of N-linked glycosylation characterized by feeding problems, mild-...

A novel mutation and first report of dilated cardiomyopathy in ALG6-CDG (CDG-Ic): a cas...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861021
Orphanet Journal of Rare Diseases; Al-Owain M, Mohamed S et. al.

Apr 19th, 2010 - Congenital disorders of glycosylation (CDG) are an expanding group of inherited metabolic diseases with multisystem involvement. ALG6-CDG (CDGIc) is an endoplasmatic reticulum defect in N-glycan assembly. It is usually milder than PMM2-CDG (CDG-Ia...

see more →

Clinicaltrials.gov  2 results

ALG6-CDG (CDG-Ic)
https://rarediseases.info.nih.gov/diseases/9829/alg6-cdg-cdg-ic

Jun 30th, 2016 - The following summary is from Orphanet, a European reference portal for information on rare diseases and orphan drugs. Orpha Number: 79320 Definition A form of congenital disorders of N-linked glycosylation characterized by feeding problems, mild-...

A novel mutation and first report of dilated cardiomyopathy in ALG6-CDG (CDG-Ic): a cas...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861021
Orphanet Journal of Rare Diseases; Al-Owain M, Mohamed S et. al.

Apr 19th, 2010 - Congenital disorders of glycosylation (CDG) are an expanding group of inherited metabolic diseases with multisystem involvement. ALG6-CDG (CDGIc) is an endoplasmatic reticulum defect in N-glycan assembly. It is usually milder than PMM2-CDG (CDG-Ia...

see more →