Osteoporosis, Fractures, and Blindness Due to a Missense Mutation in the LRP5 Receptor.
FEVR
LRP5
familial exudative vitreoretinopathy
gracile bones
low-density lipoprotein receptor-related protein 5
skeletal dysmorphogenesis
Journal
Orthopedic research and reviews
ISSN: 1179-1462
Titre abrégé: Orthop Res Rev
Pays: New Zealand
ID NLM: 101531415
Informations de publication
Date de publication:
2023
2023
Historique:
received:
03
12
2022
accepted:
16
03
2023
medline:
30
3
2023
entrez:
29
3
2023
pubmed:
30
3
2023
Statut:
epublish
Résumé
Familial exudative vitreoretinopathy (FEVR) is a genetic disorder whose presentation can include osteoporosis, multiple fractures, and incomplete retinal angiogenesis leading to retinal detachment and blindness if left untreated. Discussed herein are the cases of two pediatric siblings who presented to the orthopedic service with multiple fractures and, through interdisciplinary management, were diagnosed with FEVR and treated appropriately before permanent visual impairment. The skeletal manifestations of FEVR, which have not been explored in depth in prior literature, are described. One sibling presented to orthopedic services for evaluation of a closed distal radius fracture sustained while playing sports. A comprehensive history revealed he had suffered at least four appendicular fractures in his lifetime, and dual-energy x-ray absorptiometry (DEXA) scan revealed his bone density to be in the first percentile for his age. Concurrent evaluation of his younger sibling revealed a similar history of multiple fractures and low bone density. Referral to genetic services and ensuing whole-exome sequencing revealed a likely pathogenic variant in both siblings'
Identifiants
pubmed: 36987449
doi: 10.2147/ORR.S400111
pii: 400111
pmc: PMC10040166
doi:
Types de publication
Case Reports
Langues
eng
Pagination
39-45Informations de copyright
© 2023 Littman et al.
Déclaration de conflit d'intérêts
The authors report no conflicts of interest in this work.
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