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This Concept Map, created with IHMC CmapTools, has information related to: Jakob B. and Maitland, CDG is caused by a defective PMM2 gene, CDG symptoms for adults include joint deformities, it is a reccessive trait that requires both parents to have mutations in the PMM2 gene, Defective DNA and currently there is no treatment for the disease, the symptoms inside the cytoplasm, enzymes that bond sugars, CDG symptoms for adults include loss of sight, PMM2 gene which orders the making of enzymes, cytoplasm inside of almost all different types of cells in the body, proteins and sugars, Females do not go through puberty due to the slowing down of maturation rate, and symptoms for infants include eyes do not look in the same direction, no treatment for the disease but there is treatment for some of the symptoms, joint deformities also Females do not go through puberty, CDG symptoms for infants include failure to grow at expected rate, treatment for some of the symptoms studies for treatments are not being researched due to lack of interest, loss of sight also Females do not go through puberty, and symptoms for infants include delay in development, mental handicap also Females do not go through puberty, and symptoms for infants include weak muscles