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A Rare Case of Complete Cryptophthalmos and Suspected Fraser’s Syndrome in a Female Neonate [PDF]
Clinical Medicine Insights: Case Reports, 2023 Cryptophthalmos is a rare congenital eye anomaly characterized by the absence of the palpebral fissure. Cryptophthalmos is often associated with Fraser’s syndrome.
Tarun Kumar Suvvari +2 more
exaly +3 more sources
Clinical features and orbital anomalies in Fraser syndrome and a review of management options [PDF]
Indian Journal of Ophthalmology, 2022 Purpose: Fraser syndrome is a rare congenital disorder comprising cryptophthalmos, syndactyly, and many times, urogenital anomalies. Herein, the authors aimed to study and report the clinical features and orbital anomalies in cases diagnosed with Fraser ...
Deepsekhar Das +4 more
doaj +3 more sources
Indian Journal of Ophthalmology, 1990 A rare case of unilateral cryptophthalmos have unique findings is reported. The lateral part of the left eye was replaced by downward extension of the frontal hairline.
Gupta V, Sen D
doaj +3 more sources
Cryptophthalmos: Associated Syndromes and Genetic Disorders
Ophthalmic Genetics, 2023 Cryptophthalmos is a rare congenital condition caused by anomalous eyelid development where the eyelid folds do not develop or fail to separate. Cryptophthalmos can be unilateral or bilateral and can occur in isolation or as part of an underlying syndrome.
Alanna Strong, Daphna Prat, Diana H Kim
exaly +3 more sources
FRASER SYNDROME: A CASE REPORT
Khyber Medical University Journal, 2021 Fraser syndrome (cryptophthalmos syndrome) is a congenital anomaly in which cryptophthalmos is the main feature. Other malformations can include syndactyly, craniofacial and urogenital anomalies.
Madiha Waseem +2 more
doaj +1 more source
History and highlights of the teratological collection in the Narrenturm, Vienna (Austria)
American Journal of Medical Genetics Part A, Volume 191, Issue 5, Page 1301-1324, May 2023., 2023 Abstract The collection of the Narrenturm in Vienna houses and maintains more than 50,000 objects including approximately 1200 teratological specimens; making it one of the biggest collections of specimens from human origin in Europe. The existence of this magnificent collection―representing an important resource for dysmorphology research, mostly ...
Lucas L. Boer +8 more
wiley +1 more source
Mechanisms driving vestibular lamina formation and opening in the mouse
Journal of Anatomy, Volume 242, Issue 2, Page 224-234, February 2023., 2023 The mouse vestibular lamina (VL) extends as a thin sheet around the lower incisor region prenatally and opens postnatally to create a deep lower vestibule. Apoptosis thins the extending lamina while opening starts with the formation of small pockets during a process of terminal differentiation. Similarities and differences with human VL development are
Tengyang Qiu, Abigail S. Tucker
wiley +1 more source
Managing a Case of a Congenital Cystic Eyeball: Case Report with Review of Literature
Case Reports in Ophthalmological Medicine, Volume 2022, Issue 1, 2022., 2022 A congenital cystic eyeball is an extremely rare condition, with only 52 cases reported in the literature to date. An orbital cyst replaces the eyeball which occurs due to the complete or partial failure in invagination of the primary optic vesicle during the fourth week of gestation.
Aashish Raj Pant +4 more
wiley +1 more source