Results 71 to 80 of about 795,090 (143)
Harlequin Syndrome With Hemifacial Atrophy: A Case Study
Harlequin syndrome is an autonomic syndrome of heat, emotion and exercise induced flushing and sweating limited to one side of the face in combination with impairment of sweating and flushing on the contralateral side.
Polat, Mualla +3 more
core +1 more source
The retinopathy in association with malaria fever described so far includes retinal hemorrhages, vessel changes, retinal discoloration/whitening and papilledema.
Aditya Verma, M S Krishna
doaj +1 more source
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
Use of cell fat mixed with platelet gel in progressive hemifacial atrophy
Progressive hemifacial atrophy, also known as Parry-Romberg syndrome, is an uncommon degenerative and poorly understood condition. It is characterized by a slow and progressive atrophy affecting one side of the face.
CERVELLI, VALERIO, Gentile P.
core +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
BACKGROUND: Progressive hemifacial atrophy, widely referred to as Parry-Romberg syndrome or Romberg's disease, is a rare pathologic process characterized by an acquired, idiopathic, self-limited, unilateral atrophy of the face, variably involving skin ...
L. Vaienti, M. Soresina, A. Menozzi
core +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
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

