Results 71 to 80 of about 98,173 (339)

Multi‐feature fusion‐based strabismus detection for children

IET Image Processing, 2023
Strabismus is a common ophthalmologic disease that affects approximately 1.19% to 5.0% of children; however if the disease is detected early it can be treated effectively.
Guiying Zhang, Wenjing Xu, Haotian Gong, Lilei Sun, Cong Li, Huicong Chen, Daoman Xiang   +6 more
doaj   +1 more source

Presence and development of strabismus in children with telecanthus, epicanthus and hypertelorism

Indian Journal of Ophthalmology, 2022
Purpose: To study the presence and development of strabismus in children with telecanthus, epicanthus, and hypertelorism. Methods: This is a prospective, longitudinal, and observational study.
Vidya S Mooss, V Kavitha, H N Ravishankar, Mallikarjun M Heralgi, Saba Aafreen   +4 more
doaj   +1 more source

Health-related quality of life and mental health in children and adolescents with strabismus – results of the representative population-based survey KiGGS

Health and Quality of Life Outcomes, 2019
BackgroundTo estimate the effect of strabismus (squinting) on mental health and health-related quality of life aspects in children and adolescents.MethodsData from the German Health Interview and Examination Survey for Children and Adolescents KiGGS ...
A. Schuster, H. Elflein, Roman M Pokora, M. Schlaud, Franz Baumgarten, M. Urschitz   +5 more
semanticscholar   +1 more source

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim, Alexsandra Christianne Malaquias, Debora Romeo Bertola, Raissa Carneiro Rezende, Laurana De Polli Cellin, Lucas Vieira Lacerda Pires, Ana Maria Santillan‐Vasconez, Antônio Marcondes Lerario, Renata da Cunha Scalco, Alexander Augusto de Lima Jorge   +9 more
wiley   +1 more source

Prevalence of Strabismus among Patients Attending Basrah Teaching Hospital, Basrah, Iraq [PDF]

Al-Anbar Medical Journal
Background: Strabismus is a relatively widespread disorder. However, there is no local relevant study examined its prevalence.Objectives: To measure the prevalence and types of strabismus.Materials and methods: The study was a hospital-based cross ...
Mohammed Al Ashoor, Hamid Al Taha
doaj   +1 more source

Orbital causes of incomitant strabismus [PDF]

, 2015
Strabismus may result from abnormal innervation, structure, or function of the extraocular muscles. Abnormalities of the orbital bones or masses within the orbit may also cause strabismus due to indirect effects on the extraocular muscles.
Lueder, Gregg T
core   +3 more sources

Prevalence of amblyopia and strabismus in Hani school children in rural southwest China: a cross-sectional study

BMJ Open, 2019
Purpose To determine the prevalence rate of amblyopia and strabismus in Chinese Hani ethnic school-aged children. Methods All grade 1 and grade 7 students in Mojiang Hani Autonomous County, located in southwest China, were invited for comprehensive eye ...
Hui Zhu, C. Pan, Qigang Sun, Dan Huang, Z. Fu, Jing Wang, Xuejuan Chen, Zijin Wang, Hu Liu   +8 more
semanticscholar   +1 more source

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young, Armelle Pindon, Maggie R. Brand, Kate Wears, Katherine H. Young, Alyssa Mendel, Michael J. Lyons   +6 more
wiley   +1 more source

Ocular manifestations in Gorlin-Goltz syndrome [PDF]

, 2019
Background: Gorlin-Goltz syndrome, also known as nevoid basal cell carcinoma syndrome, is a rare genetic disorder that is transmitted in an autosomal dominant manner with complete penetrance and variable expressivity.
Franzone, F., Giustini, S., Himmelblau, E., Iacovino, C., Lambiase, A., Mallone, F., Miraglia, E., Moramarco, A., Roberti, V.   +8 more
core   +1 more source

The Effect of Horizontal Strabismus Muscle Surgery on the Vertical Palpebral Fissure Height [PDF]

, 2023
Amany Ragab, Hanan Mohammed, Ahmed Shafik   +2 more
openalex   +1 more source