Camurati-Engelmann disease

Camurati-Englemann disease (CED) is a rare, clinically variable bone dysplasia syndrome characterized by hyperostosis of the long bones, skull, spine and pelvis, associated with severe pain in the extremities, a wide-based waddling gait, joint contractures, muscle weakness and easy fatigability. Camurati-Englemann disease (CED) is a rare, clinically variable bone dysplasia syndrome characterized by hyperostosis of the long bones, skull, spine and pelvis, associated with severe pain in the extremities, a wide-based waddling gait, joint contractures, muscle weakness and easy fatigability.

Muscle weakness

Reduced strength of muscles.

合計: 2

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PMID (PMCID)
26649122 (4661483)	OTHER
	Visual and otologic manifestation of Camurati-Engelmann's disease: a case report.
	Alam T, Khurram M, Hamidi H, Khan AA. Radiol Case Rep. 2015;10(4):61-4.
	Most patients of CED (also known as progressive diaphyseal dysplasia and oeteopathica hyperostotica multiplex infantalis) present with extremity pain, muscle weakness, and waddling gait.
2732328	MALE
	Progressive diaphyseal dysplasia presenting as neuromuscular disease.
	Stenzler S, Grogan DP, Frenchman SM, McClelland S, Ogden JA. J Pediatr Orthop. 1989;9(4):463-7.
	Two children with progressive diaphyseal dysplasia (Engelmann's disease) were initially diagnosed as having a neuromuscular disorder because of their clinical presentations of muscle weakness, a waddling gait, and limb pain.