Congenital Disorder of Glycosylation

Case study on a 14 years old girl with a very rare condition: Congenital Disorder of Glycosylation

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Case study by Teodora-Gabriela Fleseru, MD, Pediatric Resident, 1st Pediatric Clinic, Cluj-Napoca and Silaghi Ciprian, Kinesiotherapist at A smile with MIRA, Cluj-Napoca   Introduction PMM2-CDG, MPI-CDG , ALG3-CDG, RFT1-CDG,  SSR4-CDG, MOGS-CDG1, no, it’s not a secret code or letters from a crossword as you may think. CDG is a way of living for Timea (14 years old), a young girl from […]