U01.01.039 Homocystinuria
8 Total attempts
amino acid metabolism, atherosclerosis, autosomal recessive, Cardiovascular Risk, CBS Deficiency, clinical biochemistry, Cystathionine Beta Synthase, Downward Lens Dislocation, Genetics, H5P, homocysteine, Homocystinuria, Inborn Errors of Metabolism, intellectual disability, Learning Activity, lens dislocation, Marfanoid habitus, Medical Education, Medical Students, metabolic disease, metabolic disorder, methionine metabolism, Osteoporosis, pathophysiology, Pyridoxine, Question Set, Quiz, thrombosis, USMLE, Vitamin B6