Results 61 to 70 of about 772 (152)

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

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

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

Journal 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, Desoutter Aline, Deneuve Sophie, Nokovitch Lara, Chaux-Bodard Anne-Gaëlle   +4 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

JPRAS 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, Ekaterina Valerievna Orlova, Manish Kumar Yadav, Evgeny Alexandrovich Vasilyev, Mikhail Arkad’evich Mokhirev, Kseniya Sergeevna Gileva   +5 more
doaj   +1 more source

Progressive hemifacial atrophy

Dental 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, Mukund Risbud, Avinash Kshar, Arati Oka Paranjpe   +3 more
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

Indian 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, Müzeyyen Gönül, Aysun Gökçe, Mutlu Acar, Canan Gürdal   +4 more
doaj   +1 more source

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

Case 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, Shohei Egami, Tomoaki Yokoyama, Makoto Sugiura   +3 more
doaj   +1 more source

UEG Week 2025 Moderated Posters

United European Gastroenterology Journal, Volume 13, Issue S8, Page S189-S802, October 2025.
wiley   +1 more source

Oral manifestations of Parry-Romberg syndrome: A review of literature

Avicenna Journal of Medicine, 2015
Parry-Romberg syndrome (PRS) or progressive facial hemiatrophy is a developmental craniofacial disorder of unknown etiology characterized by a slowly progressive unilateral facial atrophy.
Nader A Al-Aizari, Saleh Nasser Azzeghaiby, Hashem Motahir Al-Shamiri, Shourouk Darwish, Bassel Tarakji   +4 more
doaj   +1 more source

Facial Myokymias In Parry-Romberg Syndrome [PDF]

The Neurohospitalist, 2016
PISTOIA F, PISTOIA ML, CAROLEI A, SACCO S   +3 more
openaire   +2 more sources