Osteopetrorickets Presenting with Failure to Thrive and Hypophosphatemia

Academic Article

Abstract

  • Osteopetrosis is a rare group of bone disorders characterized by defective osteoclast bone resorption causing high bone mineral density. A high bone mineral density in combination with defective skeletal mineralization results in a phenotype of osteopetrorickets. We present a rare presentation of infantile osteopetrorickets in an 8-week-old female who presented with failure to thrive, hypophosphatemia, anemia, and thrombocytopenia. A skeletal survey showed increased bone density with rachitic changes. She was found to have a homozygous T-cell immune regulator 1 (TCIRG1) pathogenic mutation consistent with osteopetrosis. This highlights the importance of a clinical suspicion of osteopetrosis with this symptom constellation.
  • Authors

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    Digital Object Identifier (doi)

    Author List

  • Freese J; Greenup E; Sunil B; Ashraf AP
  • Volume

  • 4
  • Issue

  • 6