Results 81 to 90 of about 1,419,074 (183)

Muller’s muscle fibrosis is a possible predictive factor in the outcome of Muller’s muscle-conjunctival resection

BMC Ophthalmology
Background The purpose of our prospective study is to investigate the histopathology of Muller’s muscle extracted after Muller’s Muscle-Conjunctival Resection (MMCR) and to find the relationship between histopathological findings and the outcomes of ...
Hassan Asadigandomani, Mohammad Taher Rajabi, Navid Mohsenzadeh Kermani, Zohreh Nozarian, Mohammadreza Ghaedamini, Seyed Mohsen Rafizadeh   +5 more
doaj   +1 more source

Unilateral Levator Aponeurosis Excision for Marcus Gunn Syndrome and Risk Factors of Residual Jaw Winking

Journal of Ophthalmology, 2019
Purpose. To investigate the association of ptosis, levator, and jaw winking in Marcus Gunn jaw-winking synkinesis (MGJWS), and the risk factor of preservation and outcomes of the unilateral levator excision and frontalis suspension. Methods.
Qingyao Ning, Jing Cao, Jiajun Xie, Qi Gao, Changjun Wang, Juan Ye   +5 more
doaj   +1 more source

Corneal Topographic Changes After Eyelid Ptosis Surgery

, 2016
PURPOSE: To evaluate the corneal topography and the topographic changes after ptosis surgery on patients affected by congenital and acquired blepharoptosis.
Battendieri, Remo, Caporossi, Aldo, Savino, Gustavo, Traina, Salvatore, Riso, Monica, Poscia, Andrea   +5 more
core   +1 more source

Simultaneous posterior eyelid ptosis repair and strabismus surgery: a single-stage approach

, 2023
Purpose: Blepharoptosis with coexisting strabismus can be observed in adults, and both these conditions affect cosmetic appearance and have psychosocial effects. Both also commonly require surgery, which is typically performed using a sequential approach.
Ruveyde Bolac (5763323), Mehmet Serhat Mangan (5761025), Serhat Imamoglu (4479076), Ece Turan Vural (12684632), Nursal Melda Yenerel (5762111), Merve Beyza Yildiz (12684629)   +5 more
core   +1 more source

Surgical management of hypotropia in congenital fibrosis of extraocular muscles (CFEOM) presented by pseudoptosis

Clinical Ophthalmology, 2012
Hatem A Tawfik,1 Mohammad A Rashad21Oculoplastic Service, 2Pediatric Ophthalmology Service, Ophthalmology Department, Ain Shams University, Cairo, EgyptPurpose: To describe the demographics, characteristics, management pitfalls, and outcomes of ...
Tawfik HA, Rashad MA
doaj  

Phenotypic Exploration in Patients with Heterozygous Variant in AFG3L2 Gene: A Case‐Series and Literature Review

Movement Disorders Clinical Practice, Volume 13, Issue 9, Page 2250-2258, September 2026.
Abstract Background Variants in AFG3‐Like Matrix AAA Peptidase, Subunit 2 (AFG3L2) gene are associated with diverse clinical phenotypes. Here, we describe phenotypic findings of two unrelated children with de novo heterozygous variant and one family with inherited heterozygous variant in AFG3L2 gene.
Sangeetha Yoganathan, Laura Tochen, Jacky Ganguly, Sayoni Roy Chowdhury, Haya S AlFaris, Vivek Pai, Andrea LeBlanc‐Millar, Sara Breitbart, Hrishikesh Kumar, Manohar Shroff, Arun Reginald, Grace Yoon, Alfonso Fasano, George M Ibrahim, Carolina Gorodetsky   +14 more
wiley   +1 more source

Simultaneous posterior eyelid ptosis repair and strabismus surgery: a single-stage approach

, 2022
Purpose: Blepharoptosis with coexisting strabismus can be observed in adults, and both these conditions affect cosmetic appearance and have psychosocial effects. Both also commonly require surgery, which is typically performed using a sequential approach.
Ruveyde Bolac (5763323), Mehmet Serhat Mangan (5761025), Serhat Imamoglu (4479076), Ece Turan Vural (12684632), Nursal Melda Yenerel (5762111), Merve Beyza Yildiz (12684629)   +5 more
core   +1 more source

Optical mapping reveals a higher level of large‐scale structural variants in a family with paternally transmitted myotonic dystrophy and independent Parkinson's disease

The Journal of Pathology, Volume 270, Issue 1, Page 83-97, September 2026.
Abstract Myotonic dystrophy type 1 (DM1) is a clinically challenging multisystem neuromuscular hereditary disorder, with generational increase in severity and earlier age at onset. It is caused by an unstable cytosine‐thymine‐guanine repeat expansion at the DMPK locus, accompanied by associated genetic and epigenetic modifications.
Md Mehedi Hasan, Jenna Craddock, Tingting Gong, Ruth J Lyons, Igor Stevanovski, Sanjog R Chintalaphani, Ira W Deveson, Weerachai Jaratlerdsiri, Kishore R Kumar, Vanessa M Hayes   +9 more
wiley   +1 more source

Isolated unilateral ptosis as a complication of sinusitis: A case report and literature review

Clinical Case Reports
Key Clinical Message Ptosis associated with rhinosinusitis may indicate orbital or cavernous sinus involvement, typically accompanied by various other symptoms. However, isolated ptosis is a rare occurrence. This explains the diverse treatment approaches
Youssef El Sayed Ahmad, Mohammad Abraham Kazemizadeh Gol   +1 more
doaj   +1 more source

The Rintala Advanced Modification (RAM) Flap: A Novel Technique for Off‐Centre Nasal Reconstruction

Australasian Journal of Dermatology, Volume 67, Issue 6, Page 353-359, September 2026.
ABSTRACT The traditional Rintala flap is associated with visible forehead scarring and glabellar deformities. We describe the Rintala Advanced Modification (RAM) flap, a novel technique that restricts the flap below the eyebrow line and employs asymmetric Burow's triangles for off‐centre defects.
Ramy Awadalla, Derek Davies
wiley   +1 more source