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Case Report

Infantile osteopetrosis with delayed development, organomegaly and wandering eyes: case report

ORCID Icon, , &
Received 31 Jul 2023, Accepted 20 Mar 2024, Published online: 05 Apr 2024

References

  • Yadav S, Chalise S, Chaudhary S, et al. Osteopetrosis in two siblings: two case reports. BMC Res Notes. 2016;9:55. doi: 10.1186/s13104-016-1869-x
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  • Thabet S, Almajeedi M, Mohammed M, et al. Malignant infantile osteopetrosis in a 3-year-old Yemeni child: a case report. Pan Afr Med J. 2022;43:30. doi: 10.11604/pamj.2022.43.30.36827
  • Wu CC, Econs MJ, DiMeglio LA, et al. Diagnosis and management of osteopetrosis: consensus guidelines from the osteopetrosis working group. J Clin Endocrinol Metab. 2017;102:3111–3123. doi: 10.1210/jc.2017-01127
  • Gerritsen EJ, Vossen JM, van Loo IH, et al. Autosomal recessive osteopetrosis: variability of findings at diagnosis and during the natural course. Pediatrics. 1994;93:247–253. doi: 10.1542/peds.93.2.247
  • Spinnato P, Pedrini E, Petrera MR, et al. Spectrum of skeletal imaging features in osteopetrosis: inheritance pattern and radiological associations. Genes (Basel). 2022;13:1965. doi: 10.3390/genes13111965
  • Bargujar P, Devpura K, Lora SS. Radiological signs in osteopetrosis. Indian J Endocrinol Metab. 2021;25:68–69. doi: 10.4103/ijem.ijem_125_21

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