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Partnership in the FDNA Year of Discovery

May 15, 2017 Carol Ogg, BS Pharm 2 Comments

   Not too long ago it was taught in medical school that rare diseases were just that- rare and you probably wouldn’t see a patient with a rare disease in… CONTINUE

Filed Under: Education, Partners Tagged With: Carol Ogg, Fabry, Fabry disease, Face2Gene, Facial Phenotypes, FDNA, Homocystinuria, IEM, inborn errors of metabolism, inherited metablic disorder, LSD, lysosomal storage diseases, metabolic conditions, MPS Diseases, Mucopolysaccharidosis, Rare Disease, Year of Discovery

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