Results 11 to 20 of about 27,362 (190)

Comprehensive review of amblyopia: Types and management

open access: yesIndian Journal of Ophthalmology, 2023
The optimal method of treatment for a child depends on the patient's age at the time of diagnosis, the onset and type of amblyopia, and the degree of compliance attainable. In deprivation amblyopia, the cause of visual impairment (e.g., cataract, ptosis)
Savleen Kaur   +3 more
doaj   +1 more source

Clinical Characteristics and Risk Factors of Patients with Pediatric Amblyopia

open access: yesNamık Kemal Tıp Dergisi, 2023
Aim:Amblyopia is a common disease characterized by reduced visual acuity in one or both eyes during visual development in early stages of life. Satisfactory outcomes can be achieved with early diagnosis.Materials and Methods:The study included a total of
Ali Asgar YETKİN, Abdurrahman BİLEN
doaj   +1 more source

Refractive lens replacement for refractive amblyopia: «treatment» or diagnostics?

open access: yesОфтальмохирургия, 2023
Relevance. Refractive amblyopia is one of conditions that reduce best corrected visual acuity (BCVA) in patients. With the advent of new methods of refractive surgery, we note new features of the course of refractive amblyopia in adult patients after ...
E.V. Boiko   +3 more
doaj   +1 more source

Genetic causal inference between amblyopia and perinatal factors

open access: yesScientific Reports, 2022
Amblyopia is a common visual disorder that causes significant vision problems globally. Most non-ocular risk factors for amblyopia are closely related to the intrauterine environment, and are strongly influenced by parent-origin effects.
Ju-Yeun Lee, Sangjun Lee, Sue K. Park
doaj   +1 more source

Associations between anisometropia and depth of amblyopia in Benghazi, Libya

open access: yesLibyan International Medical University Journal, 2020
Background: Amblyopia is a disorder characterized by a decrease in the best-corrected visual acuity in one or both eyes with no clear structural anomalies or ocular pathology.
Sabah Eldressi, Mariam B. Gebril
doaj   +1 more source

The Clinical Characteristics of Amblyopia in Children Under 17 Years of Age in Qassim Region, Saudi Arabia

open access: yesClinical Ophthalmology, 2022
Saeed Aljohani,1 Sulaiman Aldakhil,1 Saif H Alrasheed,2,3 Qing-Qing Tan,4 Saleh Alshammeri1 1Department of Optometry, College of Applied Medical Sciences, Qassim University, Buraydah, Qassim, Saudi Arabia; 2Department of Optometry, College of Applied ...
Aljohani S   +4 more
doaj  

Late Ophthalmologic Referral of Anisometropic Amblyopia: A Retrospective Study of Different Amblyopia Subtypes

open access: yesActa Médica Portuguesa, 2019
Introduction: Amblyopia requires a timely diagnosis and treatment to attain maximum vision recovery. Specialty literature is lacking on how early amblyopia is referred.
Maria João Vieira   +3 more
doaj   +1 more source

Amblyopia: Effectiveness of visual screening for early detection in a comparative study between urban and rural school children

open access: yesKerala Journal of Ophthalmology, 2023
Background: Amblyopia an important health problem among young children causing lifelong visual impairment if not treated at correct age. Timely screening of children for amblyopia and its appropriate treatment can prevent the consequences of the problem ...
Priti R Kapadia   +2 more
doaj   +1 more source

Amblyopia among Patients Attending the Outpatient Department of Ophthalmology of a Tertiary Care Centre: A Descriptive Cross-sectional Study

open access: yesJournal of Nepal Medical Association, 2022
Introduction: Amblyopia is defined as a reduction in visual acuity unilaterally or bilaterally without any detectable cause. It is a major public health issue in developing and underdeveloped countries. Its prevalence is usually underestimated because of
Sikshya Adhikari   +5 more
doaj   +1 more source

Respiratory Involvement in HIST1H1E‐Related Rahman Syndrome: A Case of Severe Mixed Apnea

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Rahman syndrome (HIST1H1E‐related neurodevelopmental syndrome, OMIM #617537) is a rare autosomal‐dominant condition caused by truncating variants in the C‐terminal domain of the HIST1H1E gene. It is characterized by macrocephaly, hypotonia, craniofacial anomalies, and multisystem anomalies.
Nada Barakat   +4 more
wiley   +1 more source

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