We report a patient with Cat eye syndrome (CES) associated with anatomical asplenia. To the best of our knowledge, there have been no prior reports of this association. Screening for asplenia in CES is potentially important, as asplenia places patients at increased risk for life-threatening bacterial infections. Hence patients with CES without a spleen may require the same routine precautions a...

purpose: to report a case of pseudoexfoliation syndrome in young keratoconus patient following penetrating keratoplasty. case report: a 37 year old man who underwent penetrating keratoplasty 13 years ago in his left eye due to keratoconus developed pseudoexfoliation (pex) syndrome in the operated eye. apart from pex material deposition on the crystalline lens ophthalmic exam was within normal l...

introduction cri du chat syndrome is a rare genetic disorder due to deletion of variable length of short arm of chromosome 5(5p). it mainly presents with typical cat like cry, facial dysmorphism, poor growth with feeding problems and severe cognitive, speech, and motor delays. case report we present here a one year old child who did not presented with typical features but presented with recurre...

This paper proposes a cat-eye effect target recognition method with compressive sensing (CS) and presents a recognition method (sample processing before reconstruction based on compressed sensing, or SPCS) for image processing. In this method, the linear projections of original image sequences are applied to remove dynamic background distractions and extract cat-eye effect targets. Furthermore,...

Parinaud's oculoglandular syndrome (PCOS) is a rare eye disease caused by different etiological agents, including bacteria, viruses and fungi. PCOS special form of granulomatous conjunctivitis often associated with cat scratch disease, herpes simplex infection, sporotrichosis, blastomycosis, coccidioidomycosis. Sporotrichosis subcutaneous mycosis the fungus Sporothrix schenckii global distribut...

Introduction Cri du chat syndrome is a rare genetic disorder due to deletion of variable length of short arm of chromosome 5(5p). It mainly presents with typical cat like cry, facial dysmorphism, poor growth with feeding problems and severe cognitive, speech, and motor delays. Case Report We present here a one year old child who did not presented with typical features but presented with recurre...