Results 71 to 80 of about 1,092 (167)
Epiretinal membrane removal in patients with Stargardt disease
Epiretinal membranes (ERMs) in Stargardt disease have been known to undergo spontaneous separation in children. Results of surgical intervention in adult patients with Stargardt disease have rarely been reported.
Muna Bhende +2 more
doaj +1 more source
Bilateral optic neuropathy and intraretinal deposits after pars plana vitrectomy in amyloidosis
Pathological examination of material from a nonextensive pars plana vitrectomy (PPV) in the right eye provided a diagnosis of nonfamilial amyloidosis in a 68-year-old woman, who presented with bilateral glass wool-like vitreous opacities. Genetic testing
Rossetti Alberto +3 more
doaj +1 more source
Loop myopexy with true muscle transplantation for very large angle heavy eye syndrome patient
A 42-year-old man presenting with complaints of squint for last 20 years. His visual acuity was 20/400 in right eye (RE) and 20/30 in left eye (LE) with glasses. His refraction was RE -16.75/-2.5 D cycl 180 and LE was -14.5/-1.5 D cycl 180.
Jitendra Jethani, Sonal Amin
doaj +1 more source
Fundus imaging with a nasal endoscope
Wide field fundus imaging is needed to diagnose, treat, and follow-up patients with retinal pathology. This is more applicable for pediatric patients as repeated evaluation is a challenge.
P Mahesh Shanmugam +2 more
doaj +1 more source
Lens subluxation combined with parry-romberg syndrome: case report
Background Parry-Romberg syndrome (PRS) is a rare progressive degenerative disorder of unknown etiology. Here we report a rare case of PRS combined with lens subluxation in Eye and ENT hospital of Fudan University, Shanghai.
Yating Tang +3 more
doaj +1 more source
OBJECTIVE: To evaluate the feasibility and the therapeutic effect of orthognathic surgical procedures combined distraction osteogenesis and scapular flap for correction of progressive hemifacial atrophy.
Wang, XX +6 more
core
A case report of Parry–Romberg syndrome
Key Clinical Message Parry–Romberg syndrome is characterized by progressive dystrophy in one half of the face, which usually begins in childhood. Correct and timely diagnosis of this disease, as well as a multidisciplinary approach and timely surgical ...
Kiana Babaei +3 more
doaj +1 more source
Introduction: the progressive hemifacial atrophy or Parry-Romberg syndrome is a rare disease, of slow clinical evolution that generates atrophy of the soft tissues.
Redondo-Bermúdez César +4 more
doaj
Parry-Romberg syndrome in an adolescent: a case report on progressive hemifacial atrophy. [PDF]
Srinivasan R, Joy ST.
europepmc +1 more source

