Results 31 to 40 of about 1,773 (167)
Ocular manifestations in a patient with Dandy-Walker malformation: A case report
Radiology Case Reports, 2022 We present a unique case of a ten-month-old boy with a protruding left globe and vitreous haemorrhaging, and later being diagnosed as a case of a dandy-walker syndrome (DWS) with buphthalmos and vitreous haemorrhage.
Qirat Qurban, MBBS, FCPS, MRCS +7 more
doaj +1 more source
Buphthalmos (congenital glaucoma) in the rat [PDF]
Laboratory Animals, 1974 The spontaneous occurrence of buphthalmos in a colony of WAG inbred rats was due to the presence of a persistent pupillary membrane which interfered with the drainage of aqueous humour from the eye. The condition appears to be inherited but as yet no completely satisfactory mode of inheritance can be given.
C, Young, M F, Festing, K C, Barnett
openaire +2 more sources
Bilateral Retinoblastoma Presenting Atypically with Atrophic Bulbi and Contralateral Buphthalmos
Delhi Journal of Ophthalmology, 2019 Patients with retinoblastoma commonly present with leucocoria (56%) and strabismus (20%). Presentation in the form of phthisis bulbi or atrophic bulbi and buphthalmos in a single patient is unusual and highly suggestive of retinoblastoma and is observed ...
Siddharth Madan, Sarita Beri
doaj +1 more source
A curious case of unilateral buphthalmos: Angle-closure glaucoma secondary to uveitis in a newborn
Indian Journal of Ophthalmology. Case Reports, 2021 Unilateral secondary angle-closure glaucoma due to uveitis is a rare presentation in a neonate. While the congenital pupillary membranes present predominantly with iris and pupillary changes, glaucoma being a late presentation in a milder form. We report
Sushma Tejwani +2 more
doaj +1 more source
Bilateral congenital stromal iris cyst with secondary glaucoma
American Journal of Ophthalmology Case Reports, 2022 Purpose: To report a case of bilateral congenital stromal iris cyst in a neonate. Observations: A one-month-old male child was brought with complaints of watering in both eyes and enlargement of the left eye since birth.
Toshit Varshney +4 more
doaj +1 more source
A newborn with a rare association of various congenital skin disorders – Question
Journal of Pediatric and Neonatal Individualized Medicine, 2022 We report the case of a female term neonate admitted for congenital skin anomalies to a Neonatology Department a few hours after birth. Pregnancy and vaginal delivery were uneventful.
Federico Mecarini +2 more
doaj +1 more source
Electronic Physician, 2016 Introduction: Primary congenital glaucoma (PCG) is the most common type of glaucoma in pediatric patients. The aim of this study was to compare the effectiveness of combined trabeculotomy-trabeculectomy versus Ahmed valve implantation for cases of PCG ...
Hazem Helmy
doaj +1 more source
A Case of Congenital Glaucoma in a 5-Year-Old Patient With Sturge-Weber Syndrome and Oculodermal Melanocytosis. [PDF]
Case Rep Ophthalmol MedPurpose: This study was aimed at presenting a case of Sturge–Weber syndrome and oculodermal melanocytosis in a pediatric patient and offering a viable treatment course to control the glaucoma in both eyes. Observations: A 5‐year‐old female presents with a large port‐wine stain on the left side of her face, retinal pigment changes, and diffuse slate ...
Shukla P, Habiel M.
europepmc +2 more sources
Sturge Weber Syndrome – Roach’s Type II Variant
Nepal Journal of Dermatology, Venereology & Leprology, 2020 Sturge-Weber syndrome (SWS) is a neurocutaneous sporadic disorder caused by mutation in GNAQ gene responsible for persistence of vascular plexus around cephalic portion of neural tube.
Muna Bista, Sudha Agrawal, Sweta Taparia
doaj +3 more sources
A Congenital Glaucoma Associated with Phakomatosis Pigmentovascularis in Infant Case Report
Siriraj Medical Journal, 2017 Phakomatosis Pigmentovascularis (PPV) is the rare condition which has been classified in the same spectrum with Sturge-Weber syndrome, Klippel-Trenaunay-Weber syndrome and oculodermal melanocytosis.
Sakaorat Petchyim
doaj +3 more sources