Zobrazeno 1 - 10
of 2 119
pro vyhledávání: '"anophthalmia"'
Autor:
Pooneh Nikuei, Ph.D., Zahra Khashavy, Mohammad Ali Farazi Fard, Shahrzad Tabasi4 Pharm.D. Student, Ari Zeidi5 B.Sc. Student, Parnian Pourkashani, Zahra Tabatabaei, Ebrahim Eftekhar, Mozhgan Saberi, Frouzandeh Mahjoubi
Publikováno v:
International Journal of Reproductive BioMedicine, Vol 21, Iss 8, Pp 667-672 (2023)
Abstract Background: Sex determining region Y box transcription factor 2 (SOX2) mutations lead to bilateral anophthalmia with autosomal dominant human inheritance. SOX2 mutations could result in severe ocular phenotypes usually associated with variab
Externí odkaz:
https://doaj.org/article/7477202e018c48f4a7ae1e39de3a5b01
Publikováno v:
Phyllomedusa: Journal of Herpetology, Vol 22, Iss 2 (2023)
Externí odkaz:
https://doaj.org/article/1420f71341e04d109b6213a662e2daaf
Publikováno v:
Indian Journal of Dental Research, Vol 34, Iss 3, Pp 335-338 (2023)
The absence of eye and irradiation post-enucleation may result in problems like dryness of the eye sockets, itching and crusting. This may lead to poor prosthesis adaptation and a lack of patient acceptance of the prosthesis. To combat the most commo
Externí odkaz:
https://doaj.org/article/1e77f31bb6b04fafa8e4f74201868d0e
Publikováno v:
Journal of Plastic and Reconstructive Surgery, Vol 2, Iss 1, Pp 20-24 (2023)
Clinical congenital anophthalmia causes facial asymmetry and difficulty in wearing ocular prostheses due to underdevelopment of the orbits. Orbital expansion must be started early after birth for treatment, but consensus regarding the treatment for c
Externí odkaz:
https://doaj.org/article/328f8a6b5abd42e4948ce40b8be30f94
Publikováno v:
Indian Journal of Ophthalmology, Vol 71, Iss 3, Pp 935-940 (2023)
Purpose: Hereditary causes are an important etiological category of childhood blindness. This study reports the real-world experience of a developing ocular genetic service. Methods: The study was carried out from Jan 2020 to Dec 2021 jointly by the
Externí odkaz:
https://doaj.org/article/ef831a6fea8844e6a5e58c5485692915
Autor:
Juan Seva, José Manuel Sanes, Juan Manuel Bueno, Carlos De Jódar, Marta Soler, Alejandro Bayón, Ester Párraga‐Ros
Publikováno v:
Clinical Case Reports, Vol 11, Iss 5, Pp n/a-n/a (2023)
Abstract This study describes a case of a 20‐day‐old male fighting bull with bilateral clinical anophthalmia and brachygnathia superior whose dam was 12.5 years old and was mistakenly dewormed with ivermectin intramuscularly in the first third of
Externí odkaz:
https://doaj.org/article/e4ba91cb643442feaa4e905a27a19a50
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 13 (2023)
PurposeTo explore the changes of bacterial flora in anophthalmic patients wearing ocular prosthesis (OP) and the microbiome diversity in conditions of different OP materials.MethodsA cross-sectional clinical study was conducted, involving 19 OP patie
Externí odkaz:
https://doaj.org/article/e2bcd61f6ee9423d8da0f6b95141d18c
Autor:
Ezinne Obioma Onebunne, Mary Ogbenyi Ugalahi, Bolutife Ayokunnu Olusanya, Aderonke Mojisola Baiyeroju
Publikováno v:
Nigerian Journal of Medicine, Vol 31, Iss 1, Pp 106-109 (2022)
This is a report of two cases of patients with bilateral congenital anophthalmos who presented to a tertiary hospital, in Ibadan Southwest Nigeria, with the aim of highlighting the need for increased implementation of fetal anomaly scans coverage dur
Externí odkaz:
https://doaj.org/article/2f3c6ca02160406f9558c83336a7107c
Autor:
Kreshnike Dedushi, Fjolla Hyseni, Juna Musa, Kristi Saliaj, Valon Vokshi, Ali Guy, Atiq Bhatti, Abdur Rahman, Muhammad Tahir, Loran Rakovica, Masum Rahman, Jeton Shatri
Publikováno v:
Radiology Case Reports, Vol 16, Iss 12, Pp 3772-3775 (2021)
Anophthalmia is a rare genetic disorder. It is defined as the absence of one or both eyes in a patient. It can be unilateral or bilateral. Based on the absence of anatomical structures, it is divided into primary, secondary, and degenerative anophtha
Externí odkaz:
https://doaj.org/article/c569e02cc744456d9d31d325b5daa72f
Autor:
Rabia Basharat, Kim Rodenburg, María Rodríguez-Hidalgo, Afeefa Jarral, Ehsan Ullah, Jordi Corominas, Christian Gilissen, Syeda Tatheer Zehra, Usman Hameed, Muhammad Ansar, Suzanne E. de Bruijn
Publikováno v:
Genes, Vol 14, Iss 8, p 1573 (2023)
Anophthalmia and microphthalmia (A/M) are among the most severe congenital developmental eye disorders. Despite the advancements in genome screening technologies, more than half of A/M patients do not receive a molecular diagnosis. We included seven
Externí odkaz:
https://doaj.org/article/2bc7edaa6cc140fb968555d963fe02bc