Results 21 to 30 of about 1,012 (146)

A Complex Inflammatory Triad: A Rare Case of Parry‐Romberg Syndrome With Systemic Lupus Erythematosus and Thyroiditis

open access: yesClinical Case Reports
Parry‐Romberg Syndrome (PRS) is a rare disorder characterized by progressive unilateral facial atrophy, traditionally viewed as a localized scleroderma variant. Its rare coexistence with systemic lupus erythematosus (SLE) and autoimmune thyroiditis (AIT)
Sakib Abrar   +4 more
doaj   +2 more sources

Progressive Hemifacial Atrophy (Parry-Romberg Syndrome)

open access: yesJournal of Indian Academy of Oral Medicine and Radiology
Progressive hemifacial atrophy (PHA), also known as Parry-Romberg syndrome (PRS), is an auto-limitable condition with unknown etiology, characterized by slow and progressive hemiatrophy affecting one side of the face.
Nalini Aswath, Rajalakshmi Rakshanaa
doaj   +2 more sources

Progressive Hemifacial Atrophy Treated by Orthodontic Surgery

open access: yesOral Science International, 2005
AbstractProgressive hemifacial atrophy(PHA)is a self‐limited atrophy of subcutaneous tissues(and less frequently of hard tissues)on one side of the face. It is a sporadic, slowly progressing disease whose pathogenesis is still unknown. As a rule the asymmetry caused by PHA(usually of soft tissue)is treated by volume augmentation that involves free ...
Kodama, Yasumitsu   +5 more
exaly   +3 more sources

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

open access: yesClin 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   +4 more
europepmc   +2 more sources

PARRY ROMBERG SYNDROME [PDF]

open access: yesRomanian 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   +2 more
doaj   +1 more source

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

open access: yesJournal 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   +4 more
doaj   +1 more source

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

open access: yesStomatološki 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

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

open access: yesJournal 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   +3 more
doaj   +1 more source

Lipoenxertia autóloga no tratamento da atrofia hemifacial progressiva (síndrome de Parry-Romberg): relato de caso e revisão da literatura Autologous fat transplantation for the treatment of progressive hemifacial atrophy (Parry-Romberg syndrome: case report and review of medical literatute)

open access: yesAnais Brasileiros de Dermatologia, 2011
A Síndrome de Parry-Romberg, também conhecida como atrofia hemifacial progressiva, é uma doença rara caracterizada por lenta e progressiva atrofia de hemiface. O tratamento ofertado para a síndrome, geralmente, visa melhorar o aspecto estético.
Júlio César Garcia de Alencar   +3 more
doaj   +1 more source

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

open access: yesClinical 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   +4 more
doaj   +1 more source

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