Results 71 to 80 of about 108,719 (194)
Acta Ophthalmologica, EarlyView.Abstract Purpose Dexamethasone eye drops are being introduced off‐label to prevent progression of severe retinopathy of prematurity (ROP). We evaluated ophthalmologic outcomes in early childhood after postnatal topical dexamethasone exposure in pre‐term infants at a standardized follow‐up examination.
Mariya Petrishka‐Lozenska +3 more
wiley +1 more source
Clinical &Experimental Ophthalmology, EarlyView.ABSTRACT Background The lack of validated and sensitive clinical endpoints remains a major challenge in the design of gene therapy trials for inherited retinal dystrophies (IRDs). This prospective longitudinal cohort study describes the natural disease progression of IRDs caused by pathogenic mutations in the Crumbs homologue 1 (CRB1) gene, and ...
Jessica S. Karuntu +15 more
wiley +1 more source
Infantile nystagmus: an optometrist’s perspective
, 2017 Asma AA Zahidi, J Margaret Woodhouse, Jonathan T Erichsen, Matt J Dunn Research Unit for Nystagmus, School of Optometry and Vision Sciences, Cardiff University, Cardiff, UK Abstract: Infantile nystagmus (IN), previously known as congenital
Dunn MJ +3 more
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Deep Phenotyping in ReNU Syndrome Identifies a Recognizable Age‐Dependent Clinical Trajectory
Clinical Genetics, EarlyView.Longitudinal evaluation of 11 individuals with ReNU syndrome revealed an age‐dependent multisystem trajectory. This longitudinal description may help clinicians anticipate changing needs in feeding, growth, neurological, visual, communication, behavioral, and orthopedic care. ABSTRACT Pathogenic variants in the noncoding gene RNU4‐2 cause ReNU syndrome,
Nadja Pekkola Pacheco +14 more
wiley +1 more source
Pendular and See-saw Nystagmus in Four Patients with Achiasma
, 2023 Congenital achiasma is a rare disorder characterized by severe or total absence of crossing fibers at the optic chiasm. This disorder typically occurs in isolation, but can also be associated with septo-optic dysplasia, esophageal atresia, agenesis of ...
Randy Brown; Shannon Beres
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Clinical Genetics, EarlyView.Genetic causes of Müllerian aplasia remain largely unknown. We report the first molecularly confirmed case of Coffin–Siris syndrome 3 caused by a de novo SMARCB1 variant presenting with Müllerian aplasia, supporting a potential association between BAF complex dysfunction and abnormal Müllerian duct development. Created in BioRender. Herlin, M. K. (2026)
Anneli C. S. Bolund +5 more
wiley +1 more source
Walsh & Hoyt: Gaze-Evoked Nystagmus
, 2005 Nystagmus that is induced by turning the eye to an eccentric position in the orbit is called gaze-evoked nystagmus. It is the most common form of nystagmus encountered in clinical practice.
John R. Leigh, MD; Janet C. Rucker, MD
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Physiologic End Point Nystagmus
, 2022 This is a normal subject with end point nystagmus in lateral gaze. Features that favor physiologic (normal) end point nystagmus (EPN) rather than pathologic gaze-evoked nystagmus include: only present in far lateral gaze (at close to 100% of the normal ...
Daniel R. Gold, DO
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Clinical Otolaryngology, EarlyView.ABSTRACT Introduction This study investigated the relationship between vestibular neuritis and various systemic inflammatory indices—namely, neutrophil‐to‐lymphocyte ratio (NLR), platelet‐to‐lymphocyte ratio (PLR), monocyte‐to‐lymphocyte ratio (MLR), systemic immune‐inflammation index (SII), and systemic inflammation response index (SIRI) and the ...
Tuğba Tulacı +7 more
wiley +1 more source