Results 31 to 40 of about 1,700 (192)

Parry-Romberg syndrome: A case with a possible association with lyme disease [PDF]

open access: yes, 2015
Parry-Romberg syndrome is an acquired slowly progressive disease characterized by an atrophy mostly involving half of the face. The pathogenesis of this disfiguring condition is still controversial.
Di Meo, N.   +4 more
core   +2 more sources

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

Parry Romberg Syndrome with localized scleroderma: a case report [PDF]

open access: yes, 2014
Parry Romberg syndrome(PRS) is a rare acquired poorly understood neurocutaneous syndrome of unknown etiology characterized by slow progressive atrophic changes commonly affecting one half of the face. The exact incidence and etiology towards the syndrome
Gupta, Nikita   +3 more
core   +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

Oromandibular dystonia : a dental approach [PDF]

open access: yes, 2009
Oromandibular dystonia consists of prolonged spasms of contraction of the muscles of the mouth and jaw. Primary idiopathic forms and secondary forms exist.
Burguera Hernández, Juan Andrés   +3 more
core   +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

Scleroderma and dentistry: Two case reports [PDF]

open access: yes, 2016
© 2016 The Author(s).Background: Scleroderma is a chronic connective tissue disorder with unknown etiology. It is characterized by excessive deposition of extracellular matrix in the connective tissues causing vascular disturbances which can result in ...
Bornstein, Michael M.   +4 more
core   +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

Three-dimensional photogrammetry for surgical planning of tissue expansion in hemifacial microsomia [PDF]

open access: yes, 2010
Background: We aim to illustrate the applications of 3-dimensional (3-D) photogrammetry for surgical planning and longitudinal assessment of the volumetric changes in hemifacial microsomia. Methods.
Cheung, LK   +3 more
core   +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

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