Cargando…

Phenotype of Coats disease in females

OBJECTIVE: To determine whether the clinical presentation of Coats disease differs between males and females. METHODS AND ANALYSIS: Records of patients diagnosed with Coats disease at a single institution were retrospectively reviewed. Demographic data, main reason for initial consultation, comprehe...

Descripción completa

Detalles Bibliográficos
Autores principales:	Daruich, Alejandra, Munier, Francis L
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BMJ Publishing Group 2022
Materias:	Paediatric Ophthalmology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819807/ https://www.ncbi.nlm.nih.gov/pubmed/35141419 http://dx.doi.org/10.1136/bmjophth-2021-000883

Ejemplares similares

EVIDENCE AGAINST A CONTRALATERAL COATS PHENOTYPE BY OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY
por: Daruich, Alejandra, et al.
Publicado: (2022)

Cell-free RB1 DNA not detected in the blood of pseudoretinoblastoma patients
por: Abramson, David H, et al.
Publicado: (2022)

Pattern and prevalence of eye disorders and diseases in school-aged children: findings from the Nationwide School Sight Sampling Survey in Armenia
por: Jrbashyan, Nairuhi, et al.
Publicado: (2022)

Outcomes and surgical management of persistent fetal vasculature
por: Khandwala, Nikhila, et al.
Publicado: (2021)

Strengthening retinopathy of prematurity screening and treatment services in Nigeria: a case study of activities, challenges and outcomes 2017-2020
por: Ademola-Popoola, Dupe S, et al.
Publicado: (2021)

Visual outcomes and complications in infantile cataract surgery: a real - world scenario
por: Chattannavar, Goura, et al.
Publicado: (2022)

Evaluation of the Retinopathy of Prematurity Activity Scale (ROP-ActS) in a randomised controlled trial aiming for prevention of severe ROP: a substudy of the Mega Donna Mega trial
por: Pivodic, Aldina, et al.
Publicado: (2022)

Femtosecond laser-assisted anterior capsulotomy in children undergoing cataract surgery: a large case series
por: Trifanenkova, Irina G, et al.
Publicado: (2022)

Screen time and its correlates among children aged 3–10 years during COVID-19 pandemic in Nepal: a community-based cross-sectional study
por: Shrestha, Rajan, et al.
Publicado: (2022)

Blindness in infants presenting with advanced and untreated ROP: a single-centre study in Pakistan
por: Moin, Muhammad, et al.
Publicado: (2022)

Steroid-sparing effect of ciclosporin A 1 mg/mL: 5-year case series of 107 children and young people with vernal keratoconjunctivitis
por: Dahlmann-Noor, Annegret Hella, et al.
Publicado: (2022)

Homonymous hemianopia in childhood: a systematic scoping review protocol
por: Handley, Sian, et al.
Publicado: (2022)

Parents’ willingness to pay for children’s spectacles in Cambodia
por: Burnett, Anthea, et al.
Publicado: (2021)

Amblyopia screening effectiveness at 3–4 years old: a cohort study
por: Guimaraes, Sandra, et al.
Publicado: (2021)

Comparative cohorts of retinopathy of prematurity outcomes of differing oxygen saturation: real-world outcomes
por: Choo, May May, et al.
Publicado: (2021)

Extraocular muscle resection, recession length and surgery outcome modelling in strabismus treatment: a pilot study
por: Paduca, Ala, et al.
Publicado: (2021)

Prediction of myopia onset with refractive error measured using non-cycloplegic subjective refraction: the WEPrOM Study
por: Wong, Yee Ling, et al.
Publicado: (2021)

The FASD Eye Code: a complementary diagnostic tool in fetal alcohol spectrum disorders
por: Aring, Eva, et al.
Publicado: (2021)

Novel web application for self-assessment of distance visual acuity to support remote consultation: a real-world validation study in children
por: Allen, Louise, et al.
Publicado: (2021)

Long-term outcome of primary intraocular lens implantation in bilateral congenital cataract in infants with a median age of 35 days at surgery: a case series
por: Sand, Mari Kathrine, et al.
Publicado: (2021)

Cost comparison between botulinum neurotoxin and surgery in the treatment of infantile esotropia in a tertiary public hospital
por: Mayet, Ismail, et al.
Publicado: (2021)

Ophthalmological findings in children with non-syndromic craniosynostosis: preoperatively and postoperatively up to 12 months after surgery
por: Ntoula, Evangelia, et al.
Publicado: (2021)

Visual outcomes and safety profile of intraocular lens implantation versus aphakia in children with microspherophakia with no subluxation
por: Chattannavar, Goura, et al.
Publicado: (2023)

Primary and additional treatment preference in aggressive retinopathy of prematurity and type 1 retinopathy of prematurity
por: Jang, Ji Hye, et al.
Publicado: (2023)

Is the prolongation latency of visual evoked potentials a pathological sign in children with Down’s syndrome without ocular abnormalities? Case–control study of children with Down’s syndrome
por: Utrobičić, Dobrila Karlica, et al.
Publicado: (2023)

Refractive error correction among urban and rural school children using two self-adjustable spectacles
por: Ocansey, Stephen, et al.
Publicado: (2023)

Retinopathy of prematurity among infants admitted to two neonatal intensive care units in Ethiopia
por: Sherief, Sadik Taju, et al.
Publicado: (2023)

Burden of ocular abnormalities in patients with beta thalassaemia: a cross-sectional study
por: Baig, Rashid, et al.
Publicado: (2023)

SUBFOVEAL NODULE IN COATS' DISEASE: Toward an Updated Classification Predicting Visual Prognosis
por: Daruich, Alejandra L., et al.
Publicado: (2017)

Coats' Disease Diagnosed During Adulthood
por: Mandura, Rahaf A, et al.
Publicado: (2021)

Three-Year Results of Management of Adult-Onset Coats' Disease by Possibly Targeting Placental Growth Factor
por: Alsaggaf, Khalid, et al.
Publicado: (2020)

Exudative Retinal Detachment due to Coats Disease in a Teenager with Senior-Loken Syndrome: Case Report and Review of Literature
por: Khairil-Ridzwan, Kamalul Khusus, et al.
Publicado: (2019)

Preterm nutritional intake and MRI phenotype at term age: a prospective observational study
por: Vasu, Vimal, et al.
Publicado: (2014)

Using cluster analysis to describe phenotypical heterogeneity in extremely preterm infants: a retrospective whole-population study
por: Dassios, Theodore, et al.
Publicado: (2022)

Relationships between the clinical phenotypes and genetic variants associated with the immunological mechanism in childhood idiopathic nephrotic syndrome: protocol for a prospective observational single-centre cohort study
por: Chan, Han, et al.
Publicado: (2019)

Bilateral Stellate Nonhereditary Idiopathic Foveomacular Retinoschisis (SNIFR) Incidentally Identified in a Non-Myopic Female
por: Perente, Asli, et al.
Publicado: (2023)

A Genotype-Phenotype Analysis of Usher Syndrome in Puerto Rico: A Case Series
por: Santos, David F, et al.
Publicado: (2022)

Akwenda intervention programme for children and youth with cerebral palsy in a low-resource setting in sub-Saharan Africa: protocol for a quasi-randomised controlled study
por: Saloojee, Gillian, et al.
Publicado: (2021)

Non-medial Subperiosteal Abscess in a 63-Year-Old Female: A Case Report and Literature Review
por: Alabdulrazzaq, Elaf S, et al.
Publicado: (2023)

The small eye phenotype in the EPIC-Norfolk eye study: prevalence and visual impairment in microphthalmos and nanophthalmos
por: Day, Alexander C, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_uqetb8qjo9qp27nh6hn8fnhkt5