Results 41 to 50 of about 2,197 (177)
A review of 5 years exotropia surgery outcome in Songklanagarind Hospital
Objective: To study the outcomes and factors of muscle surgery for exotropia at Songklanagarind Hospital. Material and Methods: A review was made of medical records for patients who had muscle surgery for exotropia between January 1999 and December 2003.
S. Burachokeviwat +2 more
doaj
ABSTRACT Cobalamin C (cblC) disease is the most common disorder of Vitamin B12 activation. The early‐onset form presents within the first few months of life, with some patients identified through newborn screening (NBS). However, despite early detection and optimal treatment, patient outcomes remain poor, with intellectual impairment and progressive ...
Arthavan Selvanathan +7 more
wiley +1 more source
To report convergence excess esotropia (CEET) following 0.01% atropine eye drops (Low dose atropine [LDA]). Children who developed CEET that resolved promptly after discontinuation of LDA are described.
Mihir Kothari +5 more
doaj +1 more source
Abstract There is a growing body of literature that suggests riverine fish are some of the most threatened taxa on a global scale. Similarly, the literature suggests less‐altered tributaries may offer refugia for large‐river specialists. The greater Mississippi River basin, including the Missouri River system, has been subjected to anthropogenic ...
Mitchell R. Magruder +2 more
wiley +1 more source
Clinical profile of childhood exotropia in a tertiary eye care center in North India
Purpose: To identify different types of exotropia in children less than 16 years and their clinical presentation. The secondary objective is to identify the age of onset, age of presentation, birth history, and ocular and systemic associations as well as
Jinal Gore, Soveeta Rath, Suma Ganesh
doaj +1 more source
A rare homozygous variant in the PGM2L1 gene (NM_173582.6: c.1673delC, p.Thr558Ilefs*19) was identified in a patient presenting with developmental delay, seizures, and bilateral frontotemporal subarachnoid widening. ABSTRACT Background PGM2L1 gene variants are associated with developmental delays, seizures, and various neurological and physical ...
Mengmeng Niu, Dong Wang, Shanshan Jia
wiley +1 more source
Aim: To report a case of arachnoid cyst incidentally detected in a child who initially presented with concomitant intermittent right exotropia that progressed to incomitancy.
Yen Harn Yew +2 more
doaj +1 more source
Background To compare the effect of alternate part-time patching and pencil push-up training on control ability in patients with intermittent exotropia.
Desheng Song +4 more
doaj +1 more source
Clinical trajectories and medication response in TBC1D24‐related epilepsies
Abstract Objective Biallelic variants in TBC1D24 represent a rare cause of epilepsy and neurodevelopmental disorders, including severe developmental and epileptic encephalopathies. Here, we present the first attempt to delineate the longitudinal disease histories and effectiveness of antiseizure medications (ASMs) in TBC1D24‐related disorders.
Ealing Mondragon +9 more
wiley +1 more source
Health‐related quality of life of children with strabismus
Abstract Purpose The agreement between children with strabismus and their parents on the health‐related quality of life (HRQOL) of the child is unknown. Additionally, it is unknown if physical traits pre‐dispose to a better outcome in HRQOL after strabismus surgery in children.
Lena Boulakh +5 more
wiley +1 more source

