Results 51 to 60 of about 1,560 (180)

Atypical Ophthalmic Presentation of First and Second Branchial Arch Developmental Anomaly

open access: yesDelhi Journal of Ophthalmology
First and second branchial arch anomalies encompass a group of congenital malformations that arise from defects in the embryological development of the branchial arches, structures critical to the formation of the head and neck.
Vaishali Tomar   +6 more
doaj   +1 more source

Late occurrence of granular dystrophy in bilateral keratoconus: Penetrating keratoplasty and long-term follow-up

open access: yesIndian Journal of Ophthalmology, 2011
We report a rare case of keratoconus with granular dystrophy with a follow-up of two decades, documenting the sequential presentation of two diseases confirmed by histology and genetic studies.
Varsha M Rathi   +3 more
doaj   +1 more source

Heredity in Relation to the Eye [PDF]

open access: yes, 1913
A great and steadily increasing interest in the ocular effects of heredity has arisen in recent years, and much knowledge has been acquired by the collective work of many investigators of this hitherto neglected subject. Of all the patient and productive
Libby, George Franklin
core   +2 more sources

Neonatal corneal ulcer secondary to congenital entropion [PDF]

open access: yes, 2022
PurposeTo describe a case of central corneal ulceration in a newborn secondary to congenital entropion.ObservationsCorneal ulcers during infancy are rare and may occur secondary to congenital structural anomalies, including congenital entropion.
Ashraf, Davin   +4 more
core   +1 more source

Application of ultrasound biomicro-scopy in the planning of cataract surgery in anterior megalophthalmos

open access: yesIndian Journal of Ophthalmology, 2011
Anterior megalophthalmos, a rare hereditary disorder, is macrocornea (horizontal corneal diameter more than 13 mm) in association with enlarged lens-iris diaphragm and ciliary ring.
Mohammad Ali Zare   +3 more
doaj   +1 more source

Identification of a PORCN c.1093C>T (p.Arg365Trp) Variant in a 12‐Year‐Old Girl With Goltz–Gorlin Syndrome

open access: yesClinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT We report the first female case of Goltz–Gorlin syndrome with the PORCN c.1093C>T (p.Arg365Trp) variant, previously described only in a male with Klinefelter syndrome. This case expands the known phenotypic and genotypic spectrum of FDH.
Anna Bolzon   +5 more
wiley   +1 more source

Fraser of cryptophthalmosis syndrome: A case report [PDF]

open access: yes, 2004
Fraser or cryptophthalmos syndrome is a rare autosomal recessive disorder characterized by major features such as cryptophthalmos, syndactyly, and abnormal genitalia. Consanguinity is reported in 15-24.8% of the cases.
Adibi, B.   +3 more
core  

Teratogenic effects of carbamazepine on embryonic eye development in pregnant mice

open access: yes, 2010
Background: Carbamazepine is an antiepileptic drug used widely for the treatment of epileptic seizures and neuropathic pain. Several malformations in humans, mainly neural tube defects, have been reported as a consequence of its use during pregnancy. The
Afshar, M.   +5 more
core   +1 more source

Manitoba Oculo-tricho-anal Syndrome: Complex Surgical Correction of an Extensive Upper Lid Coloboma with Congenital Symblepharon

open access: yesThe Pan-American Journal of Ophthalmology, 2017
Manitoba Oculo-tricho-anal Syndrome (MOTA) is a rare autosomal recessive disorder characterized by eyelid coloboma, cryptophthalmos, anophthalmia or microphthalmia, abnormal hair growth from scalp to eyebrow, bifid or broad nasal tip, and ...
Suzie A Kazaryan, Alejandra A Valenzuela
doaj  

Ultrasonographic Appearance of a Posterior Lenticonus in a Cat

open access: yesVeterinary Ophthalmology, Volume 29, Issue 1, January 2026.
ABSTRACT The objective of this study is to present high‐quality and up‐to‐date ocular ultrasonographic images and videos of a posterior lenticonus with concomitant mature cataract in a cat. Additionally, the clinical findings, surgical treatment, and outcome are reported for completeness and to confirm the diagnosis.
Antonella Rampazzo   +2 more
wiley   +1 more source

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