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Vision Syndrome

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https://www.readbyqxmd.com/read/30095531/successfully-improving-visual-acuity-in-keratitis-ichthyosis-deafness-syndrome-utilizing-gas-permeable-lenses-a-case-report
#1
Sasha Strul, Penny Straughn
There is currently no well-defined guideline for treatment and management of patients with keratitis-ichthyosis-deafness (KID) syndrome, and most patients will face disabling vision loss due to corneal neovascularization and cicatrization. We offer this case as an example of how we can improve visual acuity (VA) and quality of life even in advanced cases of corneal neovascularization. We showcase the use of gas-permeable (GP) contact lenses to provide useful, functional VA in a patient with long-standing visual impairment secondary to corneal neovascularization and irregularity due to KID syndrome...
August 7, 2018: Eye & Contact Lens
https://www.readbyqxmd.com/read/30088155/tgfbi-associated-corneal-dystrophy-and-nephropathy-a-novel-syndrome
#2
China Nagano, Kandai Nozu, Tomohiko Yamamura, Shogo Minamikawa, Junya Fujimura, Nana Sakakibara, Keita Nakanishi, Tomoko Horinouchi, Yoichi Iwafuchi, Sentaro Kusuhara, Wataru Matsumiya, Norishige Yoshikawa, Kazumoto Iijima
Transforming growth factor beta-induced (TGFBI)-associated corneal dystrophies are a group of inherited progressive corneal diseases. One of these TGFBI-associated corneal dystrophies is Avellino corneal dystrophy, an autosomal dominant corneal dystrophy characterized by multiple asymmetric stromal opacities that potentially impair vision. Recently, a case with corneal dystrophy complicated by nephropathy possessing a pathogenic variant of the TGFBI gene was reported for the first time. Here, we report the second case with the same condition and the same mutation in the TGFBI gene...
August 7, 2018: CEN Case Reports
https://www.readbyqxmd.com/read/30087781/paradoxical-hypertension
#3
Sreenivasa Rao Sudulagunta, Monica Kumbhat, Mahesh Babu Sodalagunta, Shiva Kumar Bangalore Raja
Posterior reversible encephalopathy syndrome (PRES) is a clinico-radiological syndrome characterized by white matter vasogenic edema affecting the posterior occipital and parietal lobes of the brain predominantly. A 48-year-old female patient presented to ER with complaints of breathlessness and developed sudden painless loss of vision while eliciting history. The patient had a heart rate of 104/min and accelerated hypertension (BP of 220/120 mm of Hg). MRI Brain showed subcortical white matter T2/Fluid-attenuated inversion recovery hyperintensities, suggestive of PRES...
July 2018: Oxford Medical Case Reports
https://www.readbyqxmd.com/read/30074939/intraocular-jarisch-herxheimer-reaction-in-lemierre-syndrome
#4
Prithvi Ramtohul, Céline Boulicot-Seguin, Caroline Marc
PURPOSE: To report an intraocular Jarisch-Herxheimer reaction induced by Lemierre syndrome antibiotherapy. METHODS: Case report. RESULTS: A 43-year-old-man presented with an acute onset of bilateral blurred vision few days after intravenous antibiotic administration for Lemierre syndrome. Best-corrected visual acuity was 20/32 in both eyes. Examination revealed bilateral cystoid macular edema and peripheral retinal vasculitis, persisting despite Lemierre syndrome recovery with antibiotics...
August 2, 2018: Retinal Cases & Brief Reports
https://www.readbyqxmd.com/read/30057393/-quality-of-life-in-patients-with-orbitopathy-single-center-experience
#5
Beata Charążka, Agnieszka Suligowska, Jan Komorowski, Agnieszka Siejka
Thyroid-associated orbitopathy is a syndrome of eye symptoms produced by immunological inflammation of soft tissues of orbit,mostly due to Graves-Basedow disease. This disease is accompanied by proptosis, oedema of lids, double vision, tearing and photophobia. These symptoms lead to significant deterioration of quality of life due to reduction of sharpness of sight and therefore worsen emotional condition of patients. AIM: The aim of study was to assess the impact of Graves orbitopathy on quality of life...
June 27, 2018: Polski Merkuriusz Lekarski: Organ Polskiego Towarzystwa Lekarskiego
https://www.readbyqxmd.com/read/30052608/the-nonsurgical-management-of-orbital-dystopia-using-refractive-lenses-and-prosthetic-shells
#6
Varajini Joganathan, Patsy Terry, Steve Wall, Jonathan H Norris
Surgical rehabilitation of orbital dystopia can be challenging. The authors demonstrate the effective use of spectacle lenses to visually correct misalignments of the globe and the orbit. Presented is a retrospective review of 4 patients undergoing aesthetic rehabilitation through use of spectacle lenses and in a number patients a cosmetic shell.Two patients with neurofibromatosis presented with inferior dystopia of the globe and orbit. A base-down prismatic lens applied to the spectacles in conjunction with a prosthetic shell successfully visually corrected the facial asymmetry and improved patients' aesthetic appearance...
July 26, 2018: Journal of Craniofacial Surgery
https://www.readbyqxmd.com/read/30050691/emerging-therapeutic-strategies-for-limbal-stem-cell-deficiency
#7
REVIEW
Ying Dong, Han Peng, Robert M Lavker
Identification and characterization of the limbal epithelial stem cells (LESCs) has proven to be a major accomplishment in anterior ocular surface biology. These cells have been shown to be a subpopulation of limbal epithelial basal cells, which serve as the progenitor population of the corneal epithelium. LESCs have been demonstrated to play an important role in maintaining corneal epithelium homeostasis. Many ocular surface diseases, including intrinsic (e.g., Sjogren's syndrome) or extrinsic (e.g., alkali or thermal burns) insults, which impair LESCs, can lead to limbal stem cell deficiency (LSCD)...
2018: Journal of Ophthalmology
https://www.readbyqxmd.com/read/30050267/posterior-reversible-encephalopathy-syndrome-after-augmentation-cystoplasty-in-a-child-with-neurogenic-bladder
#8
Mudasir Ahmad Magray, Gowhar Nazir Mufti, Nisar Ahmad Bhat, Aejaz Ahsan Baba, Mudasir Hamid Buch, Faheem Ul Hasan, Shahid Bashir Banday
Posterior reversible encephalopathy syndrome (PRES) or leukoencephalopathy syndrome was introduced into clinical practice in 1996 by Hinchey et al ., to describe unique syndrome, clinically expressed during hypertensive and uremic encephalopathy, eclampsia, and immunosuppressive therapy. Hyperperfusion with resultant disruption of the blood-brain barrier results in vasogenic edema, but not infarction, most commonly in the parieto-occipital regions. The severity of this clinical symptom varies. For example, the visual disturbance can manifest as blurred vision, homonymous hemianopsia, or even cortical blindness...
July 2018: Journal of Indian Association of Pediatric Surgeons
https://www.readbyqxmd.com/read/30046603/association-of-visual-defects-and-occlusal-molar-class-in-children
#9
Silvia Caruso, Roberto Gatto, Mario Capogreco, Alessandro Nota
Purpose: The purpose of this cross-sectional study is to evaluate the presence of any correlations between dysfunctions related to visual impairments and dental occlusion. Methods: The test group included 34 subjects (21 males and 13 females; mean age 11 ± 2 years) randomly selected with the following inclusion criteria: absence of any diagnosis for problems at visual level except those related to refractive defects, visual acuity of at least 1.0, absence of any syndrome or malformation in the craniofacial area, good general health, and absence of any systemic disease able to influence the vision or the craniofacial growth...
2018: BioMed Research International
https://www.readbyqxmd.com/read/30045315/orbital-apex-syndrome-secondary-to-aspergilloma-masquerading-as-a-paranasal-sinus-tumor-a-case-report-and-literature-review
#10
Yu-Min Chang, Yun-Hsiang Chang, Ke-Hung Chien, Chang-Min Liang, Ming-Cheng Tai, Shin Nieh, Ying-Jen Chen
RATIONALE: Orbital apex syndrome is a complex clinical disorder featuring a collection of cranial nerve deficits characterized by impairment of the extraocular muscles, the ophthalmic branch of the trigeminal nerve, and even the optic nerve. Sino-orbital aspergillosis is rare but aggressive infection. Surgical resection accompanied by antifungal medication is advised currently. PATIENT CONCERNS: We report a 61-year-old woman diagnosed as aspergilloma presenting with the characteristic manifestations and imaging features of orbital apex syndrome...
July 2018: Medicine (Baltimore)
https://www.readbyqxmd.com/read/30045283/pregnancy-induced-hypertension-related-chorioretinitis-resembling-uveal-effusion-syndrome-a-case-report
#11
Tomohito Sato, Masaru Takeuchi
RATIONALE: Pregnancy-induced hypertension (PIH) is a major cause of maternal and fetal mortality. Hypertensive choroidopathy is a preliminary sign of vasogenic edema in the choroid, and is associated with PIH. Here, we report a post-natal case of PIH-related chorioretinitis with bilateral severe serous retinal detachment (SRD) resembling uveal effusion syndrome. PATIENT CONCERNS: A 35-year-old woman was diagnosed with severe PIH at 37 weeks of pregnancy. She underwent an emergency cesarean delivery...
July 2018: Medicine (Baltimore)
https://www.readbyqxmd.com/read/30038892/transient-cortical-blindness-in-posterior-reversible-encephalopathy-syndrome-after-postpartum-eclampsia
#12
Antonio Sesar, Ivan Cavar, Anita Pusic Sesar, Irena Sesar
Posterior reversible encephalopathy syndrome (PRES) is a clinical condition that can cause different ophthalmological and neurological symptoms. Preeclampsia toxemia or eclampsia is one of the leading causes of PRES. Herein, we present a study of a 35-year old woman who gave birth to healthy twins at 35 weeks of gestation by cesarean section because of threatened preterm delivery. On the 1st postoperative day, the woman developed a severe headache, arterial hypertension, tachycardia, generalized tonic-clonic seizures, and loss of consciousness that persisted for about 2 min...
April 2018: Taiwan Journal of Ophthalmology
https://www.readbyqxmd.com/read/30034906/congenital-microphthalmic-syndrome-in-a-swine
#13
Radka Andrysikova, Titus Sydler, Dolf Kümmerlen, Wolfgang Pendl, Robert Graage, Romana Moutelikova, Jana Prodelalova, Katrin Voelter
A 17-week-old crossbred finishing pig was presented for lameness of approximately one week. Clinical evaluation, including ophthalmologic examination, revealed ataxia, partial flaccid paresis of the pelvic limbs, skin lesions at feet and claws, and severely reduced vision/blindness. Both eyes had multiple persistent pupillary membranes (iris-to-iris and iris-to-lens) and hypermature cataracts. Histopathological examination of the eyes revealed microphthalmia, microphakia with cataract formation, myovascularised membrane in the vitreous, retinal detachment, and retinal dysplasia...
2018: Case reports in veterinary medicine
https://www.readbyqxmd.com/read/30030411/silent-sinus-syndrome-an-unusual-case-of-facial-numbness
#14
Samuel Tribich, Colin J Mahoney, Nicholas W Davies
A 49-year-old man presented with a 1-week history of right facial paraesthesia with blurred vision and diplopia. Examination was normal apart from reduced facial sensation. Following appropriate neuroimaging, we considered a diagnosis of silent sinus syndrome. He underwent a middle meatal antrostomy with complete resolution of symptoms. Silent sinus syndrome results from occlusion of the osteomeatal complex, preventing normal aeration of the maxillary sinus. Maxillary sinus hypoventilation typically causes inferior displacement of the globe in the orbit (unilateral hypoglobus)...
July 20, 2018: Practical Neurology
https://www.readbyqxmd.com/read/30027153/a-rare-case-of-bilateral-spontaneous-indirect-caroticocavernous-fistula-treated-previously-as-a-case-of-conjunctivitis
#15
Shaheryar Khan, Caspar Gibbon, Steve Johns
Carotid cavernous fistula is an abnormal communication between the carotid arterial system and the cavernous sinus. We present an interesting, rare case of bilateral spontaneous 'Barrow type- C' fistula treated presumptively as conjunctivitis. A 66 year old patient presented in the eye casualty at North Devon District Hospital in January 2016, referred from her General practitioner complaining of bilateral red eyes. She was found to have large, prominently diffused and engorged scleral blood vessels on both sides along with raised intraocular pressures of 26mm of Hg bilaterally...
January 2018: Therapeutic advances in ophthalmology
https://www.readbyqxmd.com/read/30021813/distinct-clinical-characteristics-of-paraneoplastic-optic-neuropathy
#16
Quangang Xu, Wenjuan Du, Huanfen Zhou, Xin Zhang, Hongjuan Liu, Honglu Song, Xueqiong Wang, Shihui Wei
OBJECTIVE: Paraneoplastic optic neuropathy (PON) is relatively uncommon, and the visual outcomes and prognosis of this disease have not been well documented. The aim of this study was to investigate the clinical features and prognosis of antibody-mediated PON. METHODS: Clinical data were retrospectively collected from hospitalised patients diagnosed with PON at the Neuro-Ophthalmology Department at the Chinese People's Liberation Army General Hospital from January 2015 to June 2017...
July 18, 2018: British Journal of Ophthalmology
https://www.readbyqxmd.com/read/30016650/fibrillin-microfibrils-and-elastic-fibre-proteins-functional-interactions-and-extracellular-regulation-of-growth-factors
#17
REVIEW
Jennifer Thomson, Mukti Singh, Alexander Eckersley, Stuart A Cain, Michael J Sherratt, Clair Baldock
Fibrillin microfibrils are extensible polymers that endow connective tissues with long-range elasticity and have widespread distributions in both elastic and non-elastic tissues. They act as a template for elastin deposition during elastic fibre formation and are essential for maintaining the integrity of tissues such as blood vessels, lung, skin and ocular ligaments. A reduction in fibrillin is seen in tissues in vascular ageing, chronic obstructive pulmonary disease, skin ageing and UV induced skin damage, and age-related vision deterioration...
July 20, 2018: Seminars in Cell & Developmental Biology
https://www.readbyqxmd.com/read/30012035/usher-syndrome-and-color-vision
#18
Anne Kurtenbach, Gesa Hahn, Christoph Kernstock, Stephanie Hipp, Ditta Zobor, Katarina Stingl, Susanne Kohl, Crystel Bonnet, Saddek Mohand-Saïd, Ieva Sliesoraityte, José-Alain Sahel, Isabelle Audo, Ana Fakin, Marko Hawlina, Francesco Testa, Francesca Simonelli, Christine Petit, Eberhart Zrenner
PURPOSE: The aim of this study is to report on the results of color vision testing in a European cohort of patients with Usher syndrome (USH). We describe the results in relation to Usher type (USH1 and USH2), age and visual acuity. METHODS AND METHODS: The color vision of 220 genetically confirmed adult USH patients, aged 18-70 years, was analyzed with one of three methods: the Farnsworth D-15 Dichotomous test (D-15) along with the Lanthony desaturated 15 Hue tests (D-15d), the Roth 28-Hue test, or the Ishihara 14-plate test...
July 17, 2018: Current Eye Research
https://www.readbyqxmd.com/read/29992277/dominant-pollinators-drive-non-random-community-assembly-and-shared-flower-colour-patterns-in-daisy-communities
#19
Jurene E Kemp, Nicola G Bergh, Muri Soares, Allan G Ellis
Background and Aims: As most plants rely on pollination for persistence in communities, pollination interactions should be important determinants of plant community assembly. Here, trait and phylogenetic null modelling approaches were combined with pollinator interaction networks to elucidate the processes structuring flower colour assembly patterns in Asteraceae communities in Namaqualand, South Africa. Methods: Plant species were assigned to flower colour pattern categories (CPCs) that incorporate the complexity of the bulls-eye colour pattern, using pollinator vision models...
July 10, 2018: Annals of Botany
https://www.readbyqxmd.com/read/29988598/fulminant-eye-infection-in-a-patient-with-nephrotic-syndrome
#20
Abhilash Koratala, Freddy R Malpartida, Rupam Ruchi
Endophthalmitis is a bacterial or fungal infection inside the eye, involving the vitreous and/or aqueous humors. High index of suspicion is required for this condition in immunocompromised patients with ocular complaints as it can worsen rapidly and lead to permanent loss of vision.
July 2018: Clinical Case Reports
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