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A Rare Case of Complete Cryptophthalmos and Suspected Fraser’s Syndrome in a Female Neonate [PDF]

open access: yesClinical 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]

open access: yesIndian 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   +4 more sources

Unilateral cryptophthalmos [PDF]

open access: yesIndian 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

FRASER SYNDROME: A CASE REPORT

open access: yesKhyber 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

Unilateral cryptophthalmos

open access: yesIndian Journal of Ophthalmology, 1981
Baijal G, Agarwal M, Chaurasia B
doaj   +2 more sources

History and highlights of the teratological collection in the Narrenturm, Vienna (Austria)

open access: yesAmerican 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

open access: yesJournal 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

open access: yesCase 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

Global birth defects app: An innovative tool for describing and coding congenital anomalies at birth in low resource settings

open access: yesBirth Defects Research, Volume 113, Issue 14, Page 1057-1073, August 15, 2021., 2021
Abstract Background Surveillance programs in low‐ and middle‐income countries (LMICs) have difficulty in obtaining accurate information about congenital anomalies. Methods As part of the ZikaPLAN project, an International Committee developed an app for the description and coding of congenital anomalies that are externally visible at birth, for use in ...
Helen Dolk   +16 more
wiley   +1 more source

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