INSTITUTO NACIONAL DE CIENCIASmonterrey, United States
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SAT-805 - Genotype-Phenotype Discordance in Familial Primary Hyperparathyroidism: Parafibromin Loss with CDC73 Germline Mutation in A Young Adult
Saturday, June 13, 20269:30 AM - 4:30 PM CT
MON-757 - When "Epilepsy" Is Hypocalcemia: Pseudohypoparathyroidism Type 1B Overshadowed by A Long-Standing Refractory Seizure Disorder
Monday, June 15, 20269:00 AM - 2:00 PM CT