Inherited Metabolic Disorders

Inherited Metabolic Disorders Bingo Card
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This bingo card has 64 words: Solute carrier organic anion transporter, 0%, Ammonia >150 umol/L and anion gap <20, parent not compliant with prescribed diet, Calcium phosphate and Carbonate, Degradation of Heme, 1/1,800, Urine smells of rancid butter or cabbages, Self harm, Phenobarbital, Heme, <1,000 worldwide, Darken to brown or black, Weaning, 6-12 mos, Increased hydration, Gaucher Disease, Ashkenazi Jews, Myopia, Oxidative stress trigger, High protein diet, No peroxisomes, 1/33 to 1/14, Sweet smelling urine, Early childhood, Frequent small meals, Myelin, Neonatal period, Persistent kidney stones, congenital skeletal deformity, monitored exercise with sucrose, Adrenoleukodystrophy (Zellweger moderate form), Autosomal recessive, Failure to thrive, Regression of motor skills, Recombinant gene therapy, Pentose phosphate pathway, 1/1,300, Hepato- splenomegaly & lactic acidosis, 50% boys; 0% girls, Galactose in school foods, Galactose-1-phosphate uridyltransferase, 25%, Heart, any age, Fructose free diet, Muscle glycogen phosphorylase, Slovakia, Hypoglycemia, infant screening, Brain MRI baseline & yearly MRI, Glycogen synthase, Hypotonia, 100% boys; girls will be carriers, DNA Testing, Valine and leucine, Hepato-splenomegaly, B12 and Iron, Tyrosinemia I, Kidney damage/ failure, Treat symptoms, Ammonia is toxic to the brain, Gargoylism, Phenylalanine hydroxylase and Elevated bilirubin.

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