Results 21 to 30 of about 1,773 (167)

Unilateral congenital buphthalmos [PDF]

BMJ Case Reports, 2015
A term female infant was born by forceps delivery after failed ventouse. There was a history of maternal fever and antenatal antibiotics. She was in good condition after birth but was noticed to have an ‘enlarged and cloudy right eye’. Elevated C reactive protein led to sepsis investigations and giving the infant intravenous antibiotics.
George T, Vasileiadis, Ourania, Frangouli   +1 more
openaire   +2 more sources

Bilateral buphthalmos associated with neonatal-onset ectropion uveae, microspherophakia and pigment dispersion

Indian Journal of Ophthalmology. Case Reports, 2021
Childhood glaucoma is a potentially blinding disease and poses crucial challenges in both diagnosis and management. We report a rare case of secondary glaucoma associated with nonacquired ocular anomalies in a 3-month infant with a family history of ...
Vijayalakshmi A Senthilkumar, R Krishnadas, A Ravichandar   +2 more
doaj   +1 more source

Primary Congenital Glaucoma among the Children Under 3 Years of Age in the Outpatient Department in a Tertiary Care Hospital: A Descriptive Cross-sectional Study

Journal of Nepal Medical Association, 2021
Introduction: Primary congenital glaucoma is a rare vision-threatening condition of children. Primary congenital glaucoma though a rare disease it is the most common cause of childhood glaucoma with potency to cause blindness.
Rakshya Panta Sitoula, Jamuna Gurung, Afaque Anwar   +2 more
doaj   +1 more source

Referral patterns of children with glaucoma and their caretakers in Northern Tanzania [PDF]

International Journal of Ophthalmology, 2020
"AIM: To describe the referral patterns of children with primary childhood glaucoma (PCG) or secondary childhood glaucoma (SCG) and their presenting symptoms in Northern Tanzania. METHODS: A retrospective observational study of children 0.48, better eye)
Achim Fieß, Furahini Godfrey, Alexander K. Schuster, Richard Bowman, Heiko Philippin   +4 more
doaj   +1 more source

ENUCLEATION IN A PATIENT WITH NEUROFIBROMATOSIS TYPE 1 WITH BUPHTHALMOS AND OCULAR DEFORMITY [PDF]

Acta Medica Iranica, 2007
To report a case of buphthalmos with neurofibromatosis (NF-1) who suffered with blindness suffered enucleation. Physical examination & histopathology were performed. Physical examination revealed Buphthalmos & vascularized cornea with lower lid ectropion
F. Asadi-Amoli, A. Ariapad S. Z. Tabatabaei   +1 more
doaj   +1 more source

Gonioscopy-assisted transluminal trabeculotomy in primary congenital glaucoma

American Journal of Ophthalmology Case Reports, 2022
Purpose: To report a case of gonioscopy-assisted transluminal trabeculotomy (GATT) in a patient with primary congenital glaucoma. Observations: A three-year-old boy who presented with buphthalmos and elevated intraocular pressure. Despite the presence of
Yunhe Song, Xiulan Zhang, Robert N. Weinreb   +2 more
doaj   +1 more source

A Rare Case of Coexistence: Discoid Lupus Erythematosus and Sturge-Weber Syndrome. [PDF]

Clin Case Rep
ABSTRACT This rare coexistence of Sturge–Weber Syndrome (SWS) and discoid lupus erythematosus (DLE) presents unique diagnostic and therapeutic challenges. It highlights potential shared environmental triggers and overlapping inflammatory mechanisms, underscoring the need for a multidisciplinary approach to management.
Efazati A, Mir Y, Pouradeli S, Abdolahinia Z, Sharifzadeh Kermani M.   +4 more
europepmc   +2 more sources

Unilateral buphthalmos, corneal staphyloma and corneal fistula caused by pathogenic variant in the PITX3 gene: a case report

BMC Ophthalmology, 2022
Introduction PITX3 has been reported to be associated with congenital cataracts, anterior segment mesenchymal dysgenesis, Peters’ anomaly, and microphthalmia.
Lin Zhou, Zhike Xu, Qianying Wu, Xin Wei
doaj   +1 more source

Congenital aniridia: European COST action ANIRIDIA-NET guidelines for diagnosis, management and care. [PDF]

Acta Ophthalmol
Abstract Congenital aniridia is a rare ocular disorder affecting the majority of eye structures and can be associated with systemic manifestations. The main visible phenotypic characteristic is the partial or complete absence of the iris; however, foveal hypoplasia is a more frequent and reliable clinical sign. Other ocular comorbidities are associated
Romano D, Romano V, Daruich A, Ferrari G, Robert M, Semeraro F, Lagali N, Bremond-Gignac D, ANIRIDIA‐NET Clinical Guidelines Working Group, Aniridia‐Europa and Geniris Working Group.   +9 more
europepmc   +2 more sources

Familial buphthalmos with spherophakia

Indian Journal of Ophthalmology, 1963
Nirankari M, Chaddah M
doaj   +2 more sources