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This Concept Map, created with IHMC CmapTools, has information related to: TL3a. Galactosemia, Tested in newborns differential G, Prenatally include DNA tests, Galactose 1 Phosphate into Glucose 1-phosphate, Enzyme linked fluorometric methods bad ɝ% Enz Activity, Deficiencies of Galtokinase (GALK), chronic problems later in life including Ovarian problems, Tested in newborns if detected Early treatment, GALACTOSEMIA treatment Testing Parents who may be heterozygous, Transferse turns Galactose 1 Phosphate, UDP- Glucose into Glucose 1-phosphate, DNA tests note Specificity of mutation needed, GALACTOSEMIA treatment Calcium supplements (500 mg-1000mg), More severe Symptoms Intestinal Sepsis, accumulation of galacticol in Urine, Deficiencies of Galactose-1-phosphate (GALT), Galactose 1 Phosphate inhibit Gluose-1-P- pyrophosphorylase, Dried erythrocytes using Enzyme linked fluorometric methods, Enzyme linked fluorometric methods if bad followup tests Note, if Galactose1P is bad, but GALT is good consider GALE, UDP-Galactose-4- Epimerase (GALE) Defect results in accumulation Galactose 1 Phosphate, Tested in newborns characterizations Classic (0% Activity