Results 81 to 90 of about 14,321 (288)
Congenital ectropion uveae (CEU) with refractory glaucoma: Early trabeculectomy saves vision
European Journal of Ophthalmology, 2019 We report the case of congenital ectropion uveae in a 10-year-old boy with intractable unilateral glaucoma but no systemic association. Glaucoma in congenital ectropion uveae is often poorly responsive to medial therapy and requires surgical intervention.
Kirti Singh +5 more
semanticscholar +1 more source
Recognising cutaneous tuberculosis
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 7, Page 793-802, July 2025.Summary Tuberculosis (TB) continues to be a leading cause of death in many countries, and also remains a significant concern in Germany, particularly due to migration. The diagnosis of rare cutaneous tuberculosis is challenging as it manifests in various clinical forms that resemble more common dermatological conditions.
Cathrin Gramminger, Tilo Biedermann
wiley +1 more source
Optic nerve head recovery following the iop-lowering surgery in the eye with early juvenile glaucoma-nine years follow up [PDF]
Vojnosanitetski Pregled, 2018 Introduction. Congenital uveal ectropion (CEU) is a rare, non-progressive condition often accompanied with eyelid ptosis, anterior insertion of the iris, disgenesis of the iridocorneal angle and glaucoma. Case report.
Marković Vujica +6 more
doaj +1 more source
Ocular rhinosporidiosis mimicking conjunctival squamous papilloma in Kenya - a case report. [PDF]
, 2014 BACKGROUND: Ocular rhinosporidiosis is a chronic granulomatous infection caused by a newly classified organism that is neither a fungus nor bacterium. It often presents as a benign conjunctival tumour but may mimic other ocular conditions.
Burton, Matthew J +6 more
core +3 more sources
CONGENITAL ECTROPION UVEAE AND GLAUCOMA [PDF]
Australian and New Zealand Journal of Ophthalmology, 1985 AbstractCongenital ectropion uveae is a rare condition which may be present in one or both eyes. If the patient is followed glaucoma will always be found to be present. Associated features which have been described are ptosis, Rieger's anomaly, Prader Willi syndrome, facial hemiatrophy and neurofibromatosis.
openaire +3 more sources
Journal of Cellular and Molecular Medicine, Volume 29, Issue 14, July 2025.ABSTRACT The stability of the knee joint following anterior cruciate ligament (ACL) restoration combined with medial collateral ligament (MCL) injury repair is crucial. It is yet unknown how posterior oblique ligament (POL) suturing functions in these procedures.
Qi Ao +11 more
wiley +1 more source
Oculopatie con predisposizione di razza nel Cocker Spaniel [PDF]
, 2016 Riassunto analitico Oculopatie con predisposizione di razza nel Cocker Spaniel Lo scopo di questa tesi è stato quello di determinare la prevalenza delle oculopatie con predisposizione di razza nel Cocker Spaniel tramite uno studio retrospettivo ...
RAMAGLI, ROBERTA
core
Harlequin baby (A case report)
, 2007 In this article, a full-term male neonate with Harlequin fetus has been reported. It was born from a 20 year old mother by the Caesarean operation. In the clinical examination, broad, thick and hard hyperkeratotic disks were observed all troughs the body
Golalipour, M.J. +2 more
core +1 more source
Ichthyosis Prematurity Syndrome: A Systematic Review of the Literature
Pediatric Dermatology, Volume 42, Issue 4, Page 747-753, July/August 2025.ABSTRACT Background/Objectives Ichthyosis prematurity syndrome (IPS) is a rare autosomal recessive congenital disorder characterized by premature birth, neonatal respiratory distress, eosinophilia, and a thick, clay‐like vernix at birth. This review aims to summarize the available reported cases of IPS, including genetic etiology, clinical features ...
Grace X. Li +3 more
wiley +1 more source