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

Familial Mediterranean fever

Familial Mediterranean fever (FMF) is an autoinflammatory disorder characterized by recurrent short episodes of fever and serositis resulting in pain in the abdomen, chest, joints and muscles.

Corneal perforation

A rupture of the cornea through which a portion of the iris protrudes.

Total: 3

(per page)

PMID (PMCID)
29713855	MALE	Adult
	Case report: acute hydrops and spontaneous corneal perforation in a patient with keratoconus treated with colchicine for familial Mediterranean fever.
	Hilely A, Kleinmann G. Int Ophthalmol. 2019;39(6):1367-1369.
	Case report: acute hydrops and spontaneous corneal perforation in a patient with keratoconus treated with colchicine for familial Mediterranean fever.
29713855	MALE	Adult
	Case report: acute hydrops and spontaneous corneal perforation in a patient with keratoconus treated with colchicine for familial Mediterranean fever.
	Hilely A, Kleinmann G. Int Ophthalmol. 2019;39(6):1367-1369.
	We report a case of a 30-year-old male with keratoconus and familial Mediterranean fever treated with colchicine, presented with acute hydrops in his left eye, which progressed to a spontaneous corneal perforation.
29713855	MALE	Adult
	Case report: acute hydrops and spontaneous corneal perforation in a patient with keratoconus treated with colchicine for familial Mediterranean fever.
	Hilely A, Kleinmann G. Int Ophthalmol. 2019;39(6):1367-1369.
	To report a rare case of spontaneous corneal perforation after hydrops in keratoconus patients who suffer from familial Mediterranean fever and was treated systemically with Colchicine.