Familial aplasia of the trapezius muscle: clinical and MRI findings.

Détails

ID Serval
serval:BIB_1BECC178C955
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Institution
Titre
Familial aplasia of the trapezius muscle: clinical and MRI findings.
Périodique
Acta Paediatrica
Auteur⸱e⸱s
Newman C.J., Jacquemont S., Theumann N., Jeannet P.Y.
ISSN
1651-2227[electronic], 0803-5253[linking]
Statut éditorial
Publié
Date de publication
2011
Volume
100
Numéro
3
Pages
464-466
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: ppublish
Résumé
A 5-year-old boy was referred to our neurology clinic for suspected myopathy. His parents reported normal upper extremity strength and no limitation in daily activities; however, he was unable to raise his arms above his head. On examination, both shoulders were down-slanting and anteriorly displaced, leading to a webbed neck appearance. Muscle MRI demonstrated isolated bilateral aplasia of the trapezius muscles. His father was found to have a unilateral partial trapezius hypoplasia with no functional consequences. Conclusion:  Congenital aplasia of the trapezius muscle is a rare condition; bilateral aplasia of the muscle, having been reported in only five cases, is most often associated with aplasia of the pectoralis major. This is the first report to our knowledge to demonstrate bilateral isolated trapezius aplasia by MRI.
Pubmed
Web of science
Création de la notice
25/02/2011 19:09
Dernière modification de la notice
20/08/2019 13:52
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