Results 21 to 30 of about 795,090 (143)

Application of free serratus anterior muscle-fascial composite tissue flap and facial lipofilling in repairing progressive hemifacial atrophy

Asian Journal of Surgery
Introduction: Progressive hemifacial atrophy (PHA) is a nonnegligible disease, and its treatment currently lacks consensus. We aim to conduct an analysis of PHA patients to summarize the postoperative effect.
Xinjian Xiang, Zhengwan Jiang, Dehui Che, Gong Chen, Shichun Shen, Wenqian Ding, Yuntao Zhang, Mei Xiang, Bangzhong Zhu, Juan Xie, Dongsheng Cao   +10 more
doaj   +3 more sources

Progressive Hemifacial Atrophy With Contralateral Uveitis: A Case Report. [PDF]

Iran Red Crescent Med J, 2015
progressive atrophy of facial tissues including skin, bones and muscles. Ophthalmic disorders are common and include keratitis, uveitis, cataract, ipsilateral enophthalmos, optic neuritis, retinal vasculitis and scleral melting.
Ayyildiz O, Ayyildiz S, Durukan AH, Sobaci G.   +3 more
europepmc   +2 more sources

Neurological Manifestations of progressive hemifacial atrophy-case report

, 2022
Progressive hemifacial atrophy is a rare, unilateral, atrophic craniofacial form of morphea involving the dermis, subcutaneous tissue, fat, muscle, and even bone.
Javeria Zulfiqar, Muhammad Nadeem, Saima Manzoor, Nadia Ali Azfar   +3 more
core   +1 more source

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

Coexistence of Localized and Systemic Juvenile Scleroderma: A Case Report and Review of Literature. [PDF]

Clin Case Rep
ABSTRACT Juvenile scleroderma (JS) is a rare chronic connective tissue disorder characterized by progressive fibrosis of the skin and soft tissues with/without internal organ involvements. Scleroderma manifests itself in both systemic (SSc) and localized (LS) forms.
Miremarati A, Babaeian Roshani K, Tabrizi M, Tahghighi Sharabian F, Hoseini Nouri SA.   +4 more
europepmc   +2 more sources

Parry-Romberg Syndrome: A Case of Late Onset with Rapid Progression [PDF]

Journal of Clinical and Diagnostic Research, 2014
Parry–Romberg syndrome (PRS) or progressive hemifacial atrophy is rare, poorly understood condition with an unclear aetiology and characterized by slow and progressive atrophy affecting one side of the face.
Senthil Kumar, Dinesh Kumar, Ramesh Kumar, Rajkumar, Ramachandra Prabhakar   +4 more
doaj   +1 more source

Progressive hemifacial atrophy Parry Romberg syndrome characteristics of craniofacial morphology [PDF]

Stomatološki glasnik Srbije, 2007
The aim of this case report was to analyze clinical finding in a patient with rare, Parry Romberg syndrome. The patient was diagnosed with progressive facial hemiatrophy that affected skin, subcutaneous tissue and underlying bony structures.
Nikodijević-Latinović Angelina
doaj   +1 more source

Progressive hemifacial atrophy: Case report [PDF]

, 2006
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.
Ereno Botelho,Patrícia Cristina, Rodrigues Pinheiro,Maria das Graças, Limeira da Silveira,Carolina Souza, Viana Pinheiro,João de Jesus, da Silva Pinheiro,Thiago Pastor, Camarinha da Silva,Camila   +5 more
core   +3 more sources

Parry–Romberg syndrome associated with en coup de sabre in a patient from South Sudan – a rare entity from East Africa: a case report

Journal of Medical Case Reports, 2019
Background Parry–Romberg syndrome, also known as progressive hemifacial atrophy, is a rare degenerative disorder with numerous distinctive clinical presentations. It is usually slowly progressive, occurring more in females, and affects primarily one side
Jimmy Girgis William Abdelnour, Youeil Girgis William Abdelnour, Rose-Mery Amin Boushra Kerollos, Ziryab Imad Taha Mahmoud   +3 more
doaj   +1 more source

Trigeminal nerve electrophysiological findings in hemifacial atrophy: A systematic literature review and retrospective chart review

Clinical Neurophysiology Practice, 2021
Objective: Hemifacial atrophy (HFA) is a rare disorder characterized by progressive unilateral wasting facial soft tissue, muscle, and/or bone. Trigeminal nerve abnormalities may contribute to or result from disease pathophysiology.
Michael P. Skolka, Lisa A. Marks, Lyell K. Jones, Megha M. Tollefson, Jonathan H. Smith   +4 more
doaj   +1 more source