A common presentation of a rare genetic disorder clinically mimicking primary myopathy
Adolesc Med State Art Rev
.
2012 Aug;23(2):393-403.
Authors
K H C Wu
1
,
M R Kohn
,
A Turner
,
D O Sillence
Affiliation
1
Department of Clinical Genetics, Sydney Children's Hospital Network (Westmead), Australia.
PMID:
23162949
No abstract available
Publication types
Case Reports
Review
MeSH terms
Adolescent
Biopsy
Camurati-Engelmann Syndrome / diagnosis*
Child
Diagnosis, Differential
Diagnostic Imaging
Female
Humans
Male