Results 1 to 10 of about 1,924 (163)

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

Scientific 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, Li-Ping Dong, Chuan-Chang Dai, Jiao Wei   +3 more
doaj   +3 more sources

A case report of Parry–Romberg syndrome [PDF]

Clinical 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, Ali Rahnama, Nora Shurvarzi, Ali Movahedi   +3 more
doaj   +3 more sources

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

SAGE 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

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

BMC 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, Qinghe Jing, Yongxiang Jiang, Yi Lu   +3 more
doaj   +2 more sources

Clinical Images: Parry‐Romberg syndrome [PDF]

ACR Open Rheumatology, 2022
Aleksandra Bukiej, Winston Sequiera
doaj   +2 more sources

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

Radiology 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, Aadithiyan Sekar, Aashika Parveen Amir, Ajay Lucas Rubben Prabhu   +3 more
doaj   +2 more sources

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

Radiology 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, Suban Amatya, MD, Kriti Shrestha, MD, Shitiz Sriwastava, MD, Demetrios A. Karides, MD   +4 more
doaj   +2 more sources

Secukinumab treatment of Parry-Romberg syndrome [PDF]

JAAD Case Reports, 2020
Emily Sideris, MBBS, BA, LLB, Sally de Zwaan, MBBS (Hons), PhD, BSc (Psych), FACD   +1 more
doaj   +2 more sources

PARRY ROMBERG SYNDROME [PDF]

Romanian Journal of Rheumatology, 2016
Parry-Romberg syndrome, which is also known as progressive facial hemiatrophy, is a variant of localized scleroderma. This is a rare condition (OMIM # 141300), characterized by a progressive but self-limited atrophy of the skin and subcutaneous tissue on
Alexis-Virgil Cochino, Sigrid Covaci, Oana-Maria Farkas   +2 more
doaj   +1 more source

Parry⁃Romberg syndrome: two cases report and literature review

Chinese Journal of Contemporary Neurology and Neurosurgery, 2023
Objective Parry⁃Romberg syndrome is a rare disease characterized by unilateral facial progressive atrophy accompanied by ipsilateral intracranial lesions and/or cerebral atrophy, this article is aimed to analyze the clinical, radiological and ...
SHA Yu⁃hui, MAO Chen⁃hui, LI Sheng⁃de, ZHOU Li⁃xin, NI Jun   +4 more
doaj   +1 more source