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Duane Retraction Syndrome: A Report of Two Cases and Review of Literature.
Cureus
November 2024
Department of Ophthalmology, College of Medicine, University of Bisha, Bisha, SAU.
Stilling-Duane syndrome, a congenital condition characterized by aberrant innervation of the lateral rectus muscle and agenesis of the abducent nerve or its nucleus, results in limited horizontal eye movements. It is often misdiagnosed as acquired abducent nerve paralysis. This report highlights the importance of considering Stilling-Duane syndrome in differential diagnoses.
View Article and Find Full Text PDF[Sensory and motor clinical presentation of congenital retraction syndromes: Stilling-Duane and Brown syndrome].
J Fr Ophtalmol
May 2017
Service d'ophtalmologie, centre EVICR.net APOCHU 86, centre hospitalier universitaire Amiens-Picardie, site Sud, 80054 Amiens cedex 1, France; Université de Picardie-Jules-Verne, chemin du Thil, 80025 Amiens cedex 1, France.
Introduction: Congenital Brown syndrome and Stilling-Duane syndrome, two rare causes of strabismus are caused by fibrosis of one or more extraocular muscles. This series aims to report the clinical sensory and motor features of patients with Brown or Stilling-Duane syndrome.
Methods: Seventeen patients' records were retrospectively assessed for: the ocular deviation in primary position and in the 9 positions of gaze, head tilt, visual acuity and binocular vision.
Introduction: Duane retraction syndrome (DRS) is a congenital ocular motility disorder with innervational dysgenesis. MRI improves our understanding of this disease by providing in vivo access to nerves and oculomotor muscles. The goal of this prospective study (2000-2008) was to analyze DRS clinically and neuroradiologically.
View Article and Find Full Text PDF[Ocular coloboma associated with cervico-oculo-acoustic syndrome].
J Fr Ophtalmol
September 2006
Service d'Ophtalmologie, Hôpital Charles Nicolle, Boulevard du 9 Avril, Tunis, Tunisie.
Introduction: Cervico-oculo-acoustic syndrome is an uncommon syndrome consisting of Klippel Feil syndrome, deafness, and Duane syndrome. We relate a new case of cervico-oculo-acoustic syndrome.
Case Report: We report the case of 15-month-old girl referred for esotropia of the right eye.
Phenotypic variability in children with growth hormone deficiency associated with posterior pituitary ectopia.
Clin Endocrinol (Oxf)
April 2006
Pediatric Endocrinology and Diabetes Unit, Robert Debré Hospital, Assistance Publique--Hôpitaux de Paris, Paris VII University, France.
Objective: The cause of posterior pituitary ectopia (PPE) with anterior pituitary hormone deficiencies is unknown. This disease is usually considered sporadic. The objective of this study was to improve the phenotypic characterization of children with PPE and growth hormone deficiency (GHD) to seek insight into the mechanisms underlying abnormal pituitary-gland development.
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