Williams-Beuren Syndrome With Primary Hyperparathyroidism: A Rare Diagnosis In A Rare Genetic Syndrome

Williams-Beuren Syndrome With Primary Hyperparathyroidism: A Rare Diagnosis In A Rare Genetic Syndrome

ABSTRACT: Objective: This case report is the first to describe functional parathyroid disease in Williams-Beuren Syndrome (WBS). We report a patient with hypercalcemia in infancy and later in adulthood whose unusual complex of elfin facies and multiple medical comorbidities, including hypercalcemia,...

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Bibliographic Details
Main Authors: Julie Goswami, MD, Steven P. Hodak, MD, Sally E. Carty, MD, Kelly L. McCoy, MD
Format: Article
Language:English
Published: Elsevier 2017-01-01
Series:AACE Clinical Case Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2376060520301747

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