Results 71 to 80 of about 1,924 (163)

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

, 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., NAN, KATIUSCIA, DI MEO, NICOLA, Trevisan, G., TREVISAN, GIUSTO, STINCO, Giuseppe, Pinzani, C., Pinzani, C, Nan, K.   +8 more
core   +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

New Findings in the Parry-Romberg Syndrome: A Case Report

, 2002
PurposeTo describe further findings in the Parry-Romberg syndrome that might contribute towards a better understanding of the disease.DesignCase report.MethodsThe clinical history of a patient with the Parry-Romberg syndrome was studied, and ...
N. Rosa, SEBASTIANI, Adolfo, ROSA N., F. Ghisolfi, A. Sebastiani, BANDELLO F., GHISOLFI F., F. Bandello   +7 more
core   +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

Parry Romberg Syndrome with localized scleroderma: a case report

, 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, Negi, Raju, Khan, Mubeen, Khan, Mohsin   +3 more
core  

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

Trigeminal neuropathic pain in a patient with progressive facial hemiatrophy (Parry-Romberg syndrome)

, 2011
We reviewed the literature on published cases of progressive facial hemiatrophy (Parry-Romberg syndrome) to identify possible pathophysiological mechanisms of the ...
Goadsby, Peter J., Michele Viana, Viana, Michele, Glastonbury, Christine M., Goadsby, Peter; id_orcid, Sprenger, Till   +5 more
core   +1 more source

Intractable seizure in a case with parry-Romberg syndrome and good response to intravenous immune globulin

, 2007
Objective: Parry-Romberg syndrome is a rare disorder associated with unilateral facial atrophy involving skin, subcutaneous tissue, skeletal muscles and bone.
Farajirad, M., Ashrafzadeh, F
core   +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