Results 51 to 60 of about 755 (130)

Anesthetic Considerations of Patient with Parry Romberg Syndrome

open access: yesCase Reports in Clinical Practice, 2018
Parry Romberg syndrome is a rare progressive degenerative disease characterized by unilateral atrophy affecting the skin, connective tissue, muscle, and bone, typically occurs in children and young adults.
Sussan Soltani Mohammadi   +2 more
doaj  

Facial hemiatrophy: Review of literature and a case report

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2011
A case report of hemifacial atrophy is presented in this paper. It is also known as Parry-Romberg syndrome, is an uncommon degenerative and poorly understood condition.
Manisha S Tijare   +4 more
doaj   +1 more source

Global research status of localised scleroderma reported over the period 1993–2022: A 30‐year bibliometric analysis

open access: yesInternational Wound Journal, Volume 21, Issue 1, January 2024.
Abstract Localised scleroderma predominantly affects the skin with an unknown aetiology. Despite its clinical importance, no comprehensive bibliometric analysis has been conducted to assess the existing research landscape and future prospects for localised scleroderma. The articles related to localised scleroderma were retrieved from the WoSCC database
Zi‐Ming Li   +5 more
wiley   +1 more source

Waardenburg syndrome: A rare case

open access: yesOman Journal of Ophthalmology, 2018
Waardenburg Syndrome is a rare disorder of neural crest cell development. It is genetically inherited. Varying in prevalence from 1:42000 to 1:50,000, it compromises approximately 2-5% of congenital deaf children.
Shivlal M Rawlani   +3 more
doaj   +1 more source

Progressive facial hemiatrophy (Parry-Romberg syndrome): short case report

open access: yesJournal of Oral Medicine and Oral Surgery, 2019
Introduction: The Parry Romberg syndrome (PRS) is a mosaic disease of unknown aetiology which mostly affects women. The facial hemiatrophy generally begins during the early childhood.
Puidupin Alexandre   +4 more
doaj   +1 more source

Progressive hemifacial atrophy

open access: yesDental Research Journal, 2013
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 but self-limited atrophy affecting one side of the face.
Abhijeet Sande   +3 more
doaj   +1 more source

Parry-Romberg syndrome with multiple intracranial cysts: A rare case report

open access: yesJournal of Pediatric Neurosciences, 2016
Parry-Romberg syndrome (PRS) is a rare, poorly understood degenerative condition characterized by atrophic changes affecting one side of the face. The cause of these changes remains obscure.
Rakesh Gupta, Harshad Patil
doaj   +1 more source

An overlap case of Parry–Romberg syndrome and en coup de sabre with striking ocular involvement and anti-double-stranded DNA positivity

open access: yesIndian Journal of Ophthalmology, 2018
Parry–Romberg syndrome (PRS) may overlap localized scleroderma (morphea) lesions with linear depression (en coup de sabre [ECDS]). Overlap case with PRS and ECDS was presented.
Hatice Atas   +4 more
doaj   +1 more source

Case of Rapid Progression of Hemiatrophy on the Face: A New Clinical Entity?

open access: yesCase Reports in Dermatological Medicine, 2015
A lot of diseases, including lupus profundus, morphea, lipodystrophy, and Parry-Romberg syndrome, may manifest progressive hemifacial atrophy. These diseases usually progress slowly and rapid progression of atrophy is extremely rare.
Hisashi Nomura   +3 more
doaj   +1 more source

Preoperative planning for advanced modelling of anterolateral thigh flaps in the treatment of severe haemifacial atrophy in Parry–Romberg and Goldenhar syndrome

open access: yesJPRAS Open, 2018
Background: Technological advancement in medical science is constantly innovating solutions to the varied and complex challenges of surgery. Digital diagnostics and prospective microsurgery are rapidly evolving.
Kamil Firudinovich Abdullaev   +5 more
doaj   +1 more source

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