MRI quantitative muscle characterization in children with X-linked hypophosphatemia.
Amyotrophia
FGF23
Hypophosphatemia
Limp
MRI
Ricket
Journal
Orthopaedics & traumatology, surgery & research : OTSR
ISSN: 1877-0568
Titre abrégé: Orthop Traumatol Surg Res
Pays: France
ID NLM: 101494830
Informations de publication
Date de publication:
18 Oct 2023
18 Oct 2023
Historique:
received:
23
05
2022
revised:
20
02
2023
accepted:
23
02
2023
pubmed:
21
10
2023
medline:
21
10
2023
entrez:
20
10
2023
Statut:
aheadofprint
Résumé
Children with X Linked Hypophosphatemia (XLH) suffer from carential ricket, bone deformities and lameness. No previous study demonstrated a morphological distinction in muscles in these patients. The aim of this prospective study was to characterize, using Magnetic Resonance Imaging (MRI), the muscle morphology of pelvis, thigh and leg in children with XLH and to compare it with typically developed (TD) children. We hypothesized that lower limbs muscles in children with XLH are different from TD children and could explain limp walking. Three-dimensional reconstructions of the muscles were performed in 11 patients with XLH and 15 TD children. Muscle lengths, sections and volumes were calculated and normalized with height and weight. Mean age was 10. Lengths were all smaller in children with XLH except for the Medius/minimus gluteus muscles (p=0.64). The difference seemed higher in muscles with a long tendinous part as semitendinosus (0.139 vs 0,164; p<0.01). All volumes were significantly inferior in children with XLH. This preliminary study showed significant differences in muscle structures between patients with XLH and TD children. Medius/minimus gluteus seemed to be particularly developed in children with XLH. Nevertheless it is not possible to conclude if it is related to XLH or a consequence of bone deformities. IV.
Identifiants
pubmed: 37863188
pii: S1877-0568(23)00231-1
doi: 10.1016/j.otsr.2023.103713
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
103713Informations de copyright
Copyright © 2023 Elsevier Masson SAS. All rights reserved.