Osteopetrosis complicated by multilevel spondylolysis.
CLCN7 (chloride voltage-gated channel 7)
LRP5 (low-density lipoprotein receptor-related protein 5)
Multilevel spondylolysis
Osteopetrosis
TCIRG1 (T cell immune regulator 1)
Journal
Radiology case reports
ISSN: 1930-0433
Titre abrégé: Radiol Case Rep
Pays: Netherlands
ID NLM: 101467888
Informations de publication
Date de publication:
Apr 2024
Apr 2024
Historique:
received:
30
11
2023
revised:
02
01
2024
accepted:
04
01
2024
medline:
31
1
2024
pubmed:
31
1
2024
entrez:
31
1
2024
Statut:
epublish
Résumé
Osteopetrosis is a heterogenous group of inheritable disorders which manifests as increased bone density and brittleness. The most common and mildest variant typically presents in adulthood with bone pain and pathologic fractures, including spondylolysis. We present the case of an otherwise healthy, active 17-year-old male with a history of osteopetrosis and 1 year of chronic back pain, found to have multilevel (L1-L4) spondylolysis in the setting of severe diffuse bony sclerosis consistent with osteopetrosis. While single-level spondylolysis is an uncommon complication of osteopetrosis, multilevel spondylolysis in the pediatric population is extremely rare and the genetics of prior cases studies have not been reported. Spondylolysis should be considered as one of the types of fractures that may occur in patients with osteopetrosis.
Identifiants
pubmed: 38292800
doi: 10.1016/j.radcr.2024.01.017
pii: S1930-0433(24)00017-7
pmc: PMC10825917
doi:
Types de publication
Case Reports
Langues
eng
Pagination
1325-1328Informations de copyright
© 2024 The Authors. Published by Elsevier Inc. on behalf of University of Washington.