Blepharochalasis

It typically affects only the upper eyelids, and may be unilateral as well as bilateral.[1] Recurrent episodes of eyelid edema can be observed with spontaneous resolution.[2] Recurrent eyelid edema and inflammation are usually allergic or immune-mediated in origin.The exact etiology underlying immune system dysregulation and vascular issues causing the episodes are not yet fully understood (idiopathic).Hormonal changes are thought to contribute the blepharochalasis, which particularly occur in early adulthood (puberty).
SpecialtyDermatologyinflammationeyelidatrophyDiseases of the human eyeAdnexaChalazionBlepharitisMeibomian gland dysfunctionEntropionEctropionLagophthalmosPtosisBlepharophimosisXanthelasmaAnkyloblepharonEyelashTrichiasisMadarosisDistichiasisTrichomegalyLacrimal apparatusDacryoadenitisEpiphoraDacryocystitisXerophthalmiaExophthalmosEnophthalmosOrbital cellulitisOrbital lymphomaPeriorbital cellulitisConjunctivaChemosisConjunctivitisallergicPterygiumPseudopterygiumPingueculaSubconjunctival hemorrhageFibrous tunicScleraScleritisEpiscleritisCorneaKeratitisherpeticacanthamoebicfungalExposurePhotokeratitisCorneal ulcerThygeson's superficial punctate keratopathyCorneal dystrophyFuchs'MeesmannCorneal ectasiaKeratoconusPellucid marginal degenerationKeratoglobusTerrien's marginal degenerationPost-LASIK ectasiaKeratoconjunctivitisCorneal opacityCorneal neovascularizationKayser–Fleischer ringHaab's striaeArcus senilisBand keratopathyVascular tunicCiliary bodyUveitisIntermediate uveitisHyphemaRubeosis iridisPersistent pupillary membraneIridodialysisSynechiaChoroidChoroideremiaChoroiditisChorioretinitisFocal choroidal excavationPolypoidal choroidal vasculopathyCataractCongenital cataractChildhood cataractAphakiaEctopia lentisRetinaRetinitisCytomegalovirus retinitisRetinal detachmentPosterior vitreous detachmentRetinoschisisOcular ischemic syndromeCentral retinal vein occlusionCentral retinal artery occlusionBranch retinal artery occlusionRetinopathydiabetichypertensivePurtscher'sof prematurityBietti's crystalline dystrophyCoats' diseaseSickle cellphoticMacular degenerationRetinitis pigmentosaRetinal haemorrhageCentral serous retinopathyMacular edemaEpiretinal membraneVitelliform macular dystrophyLeber's congenital amaurosisBirdshot chorioretinopathyGlaucomaOcular hypertensionPrimary juvenile glaucomaFloaterLeber's hereditary optic neuropathyOcular hypotonyRed eyeGlobe ruptureKeratomycosisPhthisis bulbiPersistent fetal vasculaturePersistent tunica vasculosa lentisFamilial exudative vitreoretinopathyVogt-Koyanagi-Harada diseasePathwaysOptic nerveOptic discOptic neuritisoptic papillitisPapilledemaFoster Kennedy syndromeOptic atrophyOptic disc drusenOptic neuropathyIschemicanterior (AION)posterior (PION)arteritic anterior (AAION or arteritic AION)non-arteritic anterior (NAION)Kjer'sLeber's hereditaryToxic and nutritionalStrabismusExtraocular musclesBinocular visionAccommodationOphthalmoparesisChronic progressive external ophthalmoplegiaKearns–Sayre syndromepalsiesOculomotor (III)Fourth-nerve (IV)Sixth-nerve (VI)EsotropiaExotropiaHypertropiaHeterophoriaEsophoriaExophoriaCyclotropiaBrown's syndromeDuane syndromeConjugate gaze palsyConvergence insufficiencyInternuclear ophthalmoplegiaOne and a half syndromeRefractionRefractive errorHyperopiaMyopiaAstigmatismAnisometropiaAniseikoniaPresbyopiaVision disordersBlindnessAmblyopiaDiplopiaScotomaColor blindnessAchromatopsiaDichromacyMonochromacyNyctalopiaOguchi diseaseVision lossVisual impairmentAnopsiaHemianopsiabinasalbitemporalhomonymousQuadrantanopiaAsthenopiaHemeralopiaPhotophobiaScintillating scotomaAnisocoriaArgyll Robertson pupilMarcus Gunn pupilAdie syndromeMiosisMydriasisCycloplegiaParinaud's syndromeNystagmusChildhood blindnessInfectionsTrachomaOnchocerciasis