Results 51 to 60 of about 4,186 (197)
The Relevance of Blepharoptosis in Diagnostic Suspicion of Myopathies
Blepharoptosis (ptosis) is classified, based on etiology, into mechanical, cerebral, neurogenic, neuromuscular, myogenic, and due to miscellaneous causes. Primary myopathic diseases are rare causes of blepharoptosis and many patients with myogenic ptosis
Papadimas, George K. +1 more
core
We aimed to review the degree of standardization of frontalis muscle (FM)–orbicularis muscle advancement techniques in the management of severe congenital blepharoptosis and also study the evidence which supports the procedure correcting blepharoptosis ...
Kasturi Bhattacharjee +3 more
doaj +1 more source
Background and Purpose Myasthenia gravis (MG) is a complex autoimmune disorder affecting neuromuscular transmission, often leading to diagnostic and therapeutic challenges. Timely identification of “red flags” in diagnosis, therapeutic reassessment, and myasthenic crisis is crucial to optimizing patient outcomes. This Delphi‐based consensus is aimed at
Francesco Habetswallner +19 more
wiley +1 more source
PDK4 and nutrient responses explain muscle specific manifestation in mitochondrial disease
Mitochondrial disease triggers opposite responses in different muscles. Mitochondrial integrated stress response (ISRmt) and aerobic glycolysis characterize large muscles. Eye muscles show no ISRmt but activate PDK4—inhibitor of glucose oxidation—thereby upregulating beta‐oxidation, which is non‐optimal in mitochondrial disease and can explain eye ...
Swagat Pradhan +6 more
wiley +1 more source
Unrecognized side effect of statin treatment: unilateral blepharoptosis
A 43-year-old man receiving statin monotherapy (10 mg atorvastatin) for hypercholesterolemia had unilateral blepharoptosis as the result of isolated myositis of the levator muscle. Statin-induced myositis in the levator muscle should be considered in the
Ertas, Nilgun Markal +6 more
core +1 more source
OXA1L gene bi‐allelic variants cause mitochondrial myopathy. OXA1L deficiency results in combined mitochondrial respiratory chain defects and OXPHOS impairments. OXA1L deficiency leads to elevated ROS production, which may activate the NF‐κB signalling pathway, disturbing myogenic gene expression and triggering cell apoptosis. Abstract Background OXA1L
Yongkun Zhan +11 more
wiley +1 more source
ABSTRACT Objective To evaluate the safety and efficacy of Botulinum Toxin Type A (BTX‐A) injection for the treatment of tear troughs. Method This study included patients with tear troughs rated as Grade 1–2 on the Barton Aesthetic Scale, who were treated between September 2023 and September 2024.
Siyuan Zhou +8 more
wiley +1 more source
Blepharoptosis and cysticercosis
Nepal J Ophthalmol 2013; 5(10): 286 DOI: http://dx.doi.org/10.3126/nepjoph.v5i2 ...
openaire +3 more sources
ABSTRACT Localized light chain amyloidosis (loc‐AL) is a rare disorder characterized by localized deposition of misfolded AL fibrils. There are limited data on patterns of disease presentation and long‐term outcomes. In this study, we retrospectively reviewed 146 patients with loc‐AL at our institution between January 1, 2010, and March 1, 2024.
Danai Dima +11 more
wiley +1 more source
Transient and isolated neurogenic blepharoptosis after medial orbital wall reconstruction.
Neurogenic blepharoptosis related to orbital surgery is very rare and only 1 report was published in the literature. This report presents 1 case of transient and isolated neurogenic blepharoptosis after medial orbital wall reconstruction.
Lim, SY +4 more
core +1 more source

