Congenital combined eyelid imbrication and floppy eyelid syndrome: Case report and review of literature

Abstract

Congenital eyelid imbrication syndrome (CEIS) is an extremely rare, benign, transient, self-limiting eyelid malposition disorder. The classic triad of signs in patients with a CEIS consists of bilateral upper eyelids overriding the lower eyelids when child was in sleep, bilateral medial and lateral canthal tendon laxity and tarsal conjunctival hyperemia. We report a third case of congenital combined eyelid imbrication and floppy eyelid syndrome in healthy neonate that was resolved within a week with conservative treatment.

Keywords

• Posterior open globe injuries
• posterior to rectus insertion
• zone III open globe injuries
• Glaucoma severity
• juvenile glaucoma
• juvenile-onset primary open angle glaucoma
• visual field defects
• Diabetic retinopathy
• renal transplant
• visual outcome
• Gujarati
• logMAR
• repeatability
• validity
• visual acuity
• Multiple sclerosis
• optic neuritis
• optical coherence tomography
• retinal nerve fi ber layer
• visual functions
• Axon diameter
• electron microscopy
• nerve fiber layer
• oligodendrocytes
• pathology
• Frequency doubling technology perimetry
• pediatric visual field testing
• standard automated perimetry
• Central corneal thickness
• glaucoma
• pachymetry
• 20G Silicone rod
• monocanalicular stent
• canalicular laceration repair
• Coat′s like response
• pigmented paravenous chorioretinal atrophy
• Retinochoroiditis radiata
• Dacryocystectomy
• oculosporidiosis
• Rhinosporidium
• Infectious scleritis
• microbial scleritis
• ocular infection
• scleritis
• Congenital ectropion
• congenital eyelid imbrication syndrome
• congenital floppy eyelid syndrome
• congenital lax upper eyelid syndrome
• down syndrome