Results 41 to 50 of about 133 (87)

Difficult mask ventilation made easy: Three cases of Parry Romberg syndrome

Indian Journal of Anaesthesia, 2016
Parry Romberg syndrome presenting as hemifacial atrophy poses various perioperative problems due to multi-system involvement. These patients have several anaesthetic implications which are published as case reports.
Kavitha Jayaram, Indira Gurajala, Gopinath Ramachandran   +2 more
doaj   +1 more source

S2k‐Leitlinie: Diagnostik und Therapie der zirkumskripten Sklerodermie

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 4, Page 605-621, April 2024.
Zusammenfassung Die vorliegende aktualisierte S2k‐Leitlinie befasst sich mit der Diagnostik und der Therapie der zirkumskripten Sklerodermie (ZS). Diese umfasst ein Spektrum sklerotischer Erkrankungen der Haut mit, je nach Subtyp und Lokalisation, möglicher Beteiligung von hautnahen Strukturen wie Fettgewebe, Muskulatur, Gelenke und Knochen. Ein Befall
Alexander Kreuter, Pia Moinzadeh, Maria Kinberger, Gerd Horneff, Margitta Worm, Ricardo N. Werner, Andreas Hammacher, Thomas Krieg, Jörg Wenzel, Michael Oeschger, Lisa Weibel, Robert Müllegger, Nicolas Hunzelmann   +12 more
wiley   +1 more source

Progressive Hemifacial Atrophy (Parry-Romberg Syndrome)

Journal 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   +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

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

Systematic Review of Health‐Related Quality of Life Impact in Juvenile Localized Scleroderma

Arthritis Care &Research, Volume 76, Issue 3, Page 340-349, March 2024.
Objective The prevalence and types of psychosocial complications of juvenile localized scleroderma (JLS), also known as morphea, an inflammatory and sclerosing disease involving the skin, fascia, muscle, and bone, are poorly understood. Methods We performed a systematic review of literature published between 2000 and 2020 in PubMed, EMBASE, the ...
Luis F. Sanchez‐Espino, Nadia Luca, Elena Pope, Ronald M. Laxer, Andrea M. Knight, Cathryn Sibbald   +5 more
wiley   +1 more source

Hemiatrofia facial de romberg: relato de caso Romberg's facial hemiatrophy: case report

Arquivos de Neuro-Psiquiatria, 1995
Os autores apresentam o caso de uma paciente de 45 anos de idade com história de 15 meses de evolução, de hemiatrofia progressiva da face e língua à esquerda.
Nicandro De Figueiredo Neto, Johnny Wesley G. Martins, Miguel Farage Filho, Fernando Guilhon Henriques   +3 more
doaj   +1 more source

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

International 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, Tian‐Hao Li, Zhu‐Jun Li, Li‐Quan Wang, Xiao Long, Jiu‐Zuo Huang   +5 more
wiley   +1 more source

Facial hemiatrophy: Review of literature and a case report

Journal 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, Sandhya Srivastav, Rajat V Misurya, Archana H Lanje, Anil Ghom   +4 more
doaj   +1 more source

Anesthetic Considerations of Patient with Parry Romberg Syndrome

Case 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, Farideh Toorany, Abdolrahim Shahhosseini   +2 more
doaj  

Waardenburg syndrome: A rare case

Oman 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, Roshani Ramtake, Ajab Dhabarde, Sudhir S Rawlani   +3 more
doaj   +1 more source