Results 41 to 50 of about 1,773 (167)
Buphthalmos: early glaucoma history [PDF]
Glaucoma as understood today could not have been detected before the means to see the optic nerve and reliably measure the intraocular pressure were available after the mid-1850s. One form, however, manifested itself as a visible enlargement of the globe and was thus recognized since antiquity.
openaire +2 more sources
Ciliary Body Schwannoma: A Case Report and Literature Review
Purpose: To present a case of intraocular schwannoma arising from the ciliary body with description of histological and immunophenotypic characteristics.
Haythem El Mokh +4 more
doaj +1 more source
A rare case of neurofibromatosis type I with unilateral congenital ectropion uveae and glaucoma
Purpose: Neurofibromatosis Type I (NF-1) is a neurocutaneous disease affecting the skin, eye and peripheral nervous system. Congenital glaucoma is a rare association, but can be a prelude to the diagnosis of NF-1 later in life.
Prasanna Venkataraman +2 more
doaj +1 more source
ABSTRACT Purpose To evaluate the long‐term (> 1 year) outcomes of vision and intraocular pressure (IOP) control in dogs with glaucoma undergoing combined endoscopic cyclophotocoagulation (ECP) and Ahmed valve gonioimplantation (AVG). Methods Medical records between 2020 and 2025 were reviewed. Outcomes evaluated included IOP control (< 25 mmHg), vision
Sanskruti S. Potnis +6 more
wiley +1 more source
ABSTRACT A 10‐year‐old poodle with left maxillofacial osteosarcoma received volumetric modulated arc therapy delivering 32 Gy in four fractions. Treatment planning was guided by computed tomography–magnetic resonance imaging (CT–MRI) fusion for precise target delineation near the globe. Serial CT and MRI up to 12 months after treatment showed transient
Nahyun Kwon +5 more
wiley +1 more source
Klippel-Trenaunay and Sturge-Weber overlap syndrome with phakomatosis pigmentovascularis
Klippel-Trenaunay syndrome and Sturge-Weber syndrome are rare disorders with neurologic and cutaneous signs of vascular origin. Phakomatosis pigmentovascularis represents the association of widespread, aberrant, and persistent nevus flammeus and ...
Monika Chhajed +3 more
doaj +1 more source
The Homeobox Genes: Classification, Regulation, Biological Functions, and Diseases
Overview of the homeobox gene superfamily and its pathophysiological roles. The homeobox superfamily comprises several major classes, including ANTP, PRD, TALE, LIM, POU, and others. Among these, the HOX clusters (A–D) play critical roles in embryonic development specifically in conferring cellular identity, regulating morphogenesis, and guiding axial ...
Maedeh Dadzadi +5 more
wiley +1 more source
ABSTRACT Objective Evaluation of the feasibility of argon cold plasma (ACP) use in corneal diseases in clinical practice and assessment of short‐ and long‐term safety in dogs, cats, and small mammals. Animals Studied Client‐owned animals. Procedure ACP was performed in animals with corneal diseases using the kINPenVET (Neoplas GmbH, Germany) under ...
Petr Soukup, Ingrid Allgoewer
wiley +1 more source
Primary Congenital and Childhood Glaucoma—A Complex Clinical Picture and Surgical Management
Childhood glaucoma encompasses a group of rare but severe ocular disorders characterized by increased intraocular pressure (IOP), posing significant risks to vision and quality of life. Primary congenital glaucoma has a prevalence of one in 10,000–68,000
Valeria Coviltir +3 more
doaj +1 more source

