Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

Dermatomyositis

A type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness.

Raynaud phenomenon

Total: 1

(per page)

PMID (PMCID)
10616288	FEMALE	Middle Aged
	[A case of mixed connective tissue disease with microscopic polyarteritis nodosa associated with perinuclear-antineutrophil cytoplasmic antibody and anti-glomerular basement membrane].
	Inada Y, Tanaka Y, Saito K, Fujii K, Aso M, Nishino T, Awazu Y, Ota T, Eto S. Nihon Rinsho Meneki Gakkai Kaishi. 1999;22(5):342-7.
	The patient was diagnosed as mixed connective tissue disease (MCTD) based on Raynaud phenomenon, a high anti-RNP antibody level and clinical symptoms and laboratory findings suggesting SSc, dermatomyositis (DM) and systemic lupus erythematosus (SLE).