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A case report of Parry–Romberg syndrome [PDF]

open access: yesClinical Case Reports
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   +3 more sources

Late-onset Parry-Romberg Syndrome with atypical neurological manifestations: A case report [PDF]

open access: yesRadiology Case Reports
Parry-Romberg Syndrome (PRS) is a rare neurocutaneous disorder characterized by gradual facial hemiatrophy. We present a case study of a 64-year-old woman with late-onset PRS and linear scleroderma.
Sema Akkus, MD   +4 more
doaj   +5 more sources

Genetic variations in patient with Parry–Romberg syndrome [PDF]

open access: yesScientific Reports, 2023
Parry–Romberg syndrome is a rare craniofacial disorder which is characterized by progressive facial atrophy. The etiology and pathogenesis of the disease are not known. Herein, we report the genetic variants in patient with this disease.
Bao-Fu Yu   +3 more
doaj   +2 more sources

A case of parasympathetic hyperactivity and associated Parry–Romberg syndrome [PDF]

open access: yesSAGE Open Medical Case Reports, 2021
This case report describes a 46-year-old female with a history of multiple endocrine neoplasia type 1 syndrome status post-parathyroidectomy, thymectomy via robotic video-assisted thoracoscopic surgery, and pituitary adenoma resection presenting with ...
Andrea N Clapp, Anna DePold Hohler
doaj   +2 more sources

Cell-Assisted Lipotransfer for the Treatment of Parry-Romberg Syndrome [PDF]

open access: yesArchives of Plastic Surgery, 2012
Progressive facial hemiatrophy, also known as Parry-Romberg syndrome, is a progressive and self-limited deformation of the subcutaneous tissue volume on one side of the face that creates craniofacial asymmetry.
Yanko Castro-Govea   +6 more
doaj   +7 more sources

"Scleroderma linearis: hemiatrophia faciei progressiva (Parry-Romberg syndrom) without any changes in CNS and linear scleroderma "en coup de sabre" with CNS tumor [PDF]

open access: yesBMC Neurology, 2009
Background Hemifacial atrophy (Parry-Romberg syndrome) is a relatively rare disease. The etiology of the disease is not clear. Some authors postulate its relation with limited scleroderma linearis.
Brzezińska-Wcisło Ligia   +2 more
doaj   +3 more sources

Lens subluxation combined with parry-romberg syndrome: case report [PDF]

open access: yesBMC Ophthalmology
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   +2 more sources

Parry-Romberg syndrome: A case report and literature review [PDF]

open access: yesRadiology Case Reports
Parry-Romberg syndrome (PRS) is a rare neurocutaneous and craniofacial disorder characterized by progressive hemifacial wasting and atrophy that predominantly affects children and young adults, with an estimated prevalence of 1 in 700,000 individuals ...
Praveen K. Sharma   +3 more
doaj   +2 more sources

Magnetic resonance imaging findings in children with Parry-Romberg syndrome and en coup de sabre. [PDF]

open access: yesPediatr Rheumatol Online J, 2021
BACKGROUND: The aim of this study was to: (i) describe the abnormalities seen on brain imaging in a group of children with en coup de sabre (EDCS) with/without Parry-Romberg syndrome (PRS); and (ii) identify clinical predictors of brain imaging ...
Knights H   +6 more
europepmc   +3 more sources

Clinical Images: Parry‐Romberg syndrome [PDF]

open access: yesACR Open Rheumatology, 2022
Aleksandra Bukiej, Winston Sequiera
doaj   +2 more sources

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