Results 71 to 80 of about 792 (148)

Połowiczy zanik twarzy bez zmian w ośrodkowym układzie nerwowym i twardzina en coup de sabre z guzem zewnątrzmózgowym – opis przypadków

Przegląd Dermatologiczny, 2011
Introduction. Progressive facial hemiatrophy (Parry-Romberg syndrome)is a relatively rare disease of unclear aetiology. Some authorspostulate its relation with linear scleroderma.Objective.
Ligia Brzezińska-Wcisło, Anna Lis-Święty, Beata Bergler-Czop   +2 more
doaj  

En coup de sabre presenting as status epilepticus [PDF]

Clinical Rheumatology, 2020
Pawan Kashyape, Ajay Prashanth D’Souza, Basil Fathalla   +2 more
openaire   +2 more sources

Linear scleroderma as a rare cause of enophthalmos: a case report

Journal of Medical Case Reports, 2007
Introduction Enophthalmos is an important physical sign which can be easily missed. Case presentation A 64-year old female presented with painless and progressive shrinking of her right eye. Visual acuity was 6/6 in both eyes.
Fernando Bertie S, Cannon Paul S, Tumuluri Krishna, Cook Anne E   +3 more
doaj   +1 more source

Pterygium as a Potential Ocular Manifestation of Morphea: A Case Report and Pathogenic Hypothesis

Przegląd Dermatologiczny
Morphea, or localized scleroderma, is a chronic inflammatory condition marked by excessive collagen deposition, resulting in skin thickening and fibrosis.
Julia Woźna, Paweł Pazdrowski, Celina Helak-Łapaj, Maksymilian Markwitz, Adriana Polańska, Marcin Stopa, Aleksandra Dańczak-Pazdrowska   +6 more
doaj   +1 more source

An interesting case of facial en coup de sabre presenting with optic neuritis in the contralateral eye: A rare presentation

Indian Journal of Ophthalmology. Case Reports
Ocular involvement in morphea or en coup de sabre (ECS) is relatively infrequent, observed in approximately 2–3% to 14% of cases. The intricate pathogenesis underlying these ocular manifestations remains elusive.
Avinash Mishra, Mohini Agrawal, Atul Bhirud, Anchal Tripathi, Mahashweta Dash   +4 more
doaj   +1 more source

Parry–Romberg Syndrome: Radioclinical Dissociation in a Paucisymptomatic Form and a Proposed Diagnostic Framework

Diagnostics
Background and Clinical Significance: Parry–Romberg syndrome (PRS), also known as progressive hemifacial atrophy, is a rare disorder characterized by progressive unilateral hemifacial atrophy, with potential involvement of the cranial bones and the brain.
Cristian Turlea, Andrei I. Cucu, Alexandru Carauleanu, Roxana Covali, Camelia Tamas, Mihnea A. Popa, Victor Constantinescu, Anca P. Morosan, Elena Porumb-Andrese, Iulian Prutianu, Claudia F. Costea, Amelian Bobu, Adriana Hristea, Alexandru Nemtoi   +13 more
doaj   +1 more source

Co-occurrence of En Coup de Sabre, Parry-Romberg Syndrome, and Hemi Masticatory Spasm: A Case Report

Case Reports in Dermatology
Introduction: En coup de sabre (ECDS) and Parry-Romberg syndrome (PRS) are rare, localised scleroderma subtypes, often considered to be overlapping variants of morphea.
Pooja Chaurasia, Asharbh Raman, Yugal K. Sharma, Aayush Gupta   +3 more
doaj   +1 more source

Adipose Tissue Grafting for the Treatment of Morphea En Coup De Sabre: A Simple Filler or an Emerging Cellular Therapy? [PDF]

Cureus, 2022
El Omari M, Debbarh M, Lakhdari MA, Basri Z, Ait Benhamou R.   +4 more
europepmc   +1 more source

Co-occurrence of linear scleroderma en coup de sabre and segmental vitiligo on the face. [PDF]

BMJ Case Rep, 2022
Dsouza D, Kumar P, Reddy H.
europepmc   +1 more source

3D stereophotogrammetry in children and adolescents with Scleroderma En Coup De Sabre/Parry-Romberg Syndrome: Description of a novel method for monitoring disease progression. [PDF]

Skin Health Dis, 2022
Ter Horst R, Maal TJJ, de Koning MJJ, Mertens JS, Schatorjé EJH, Hoppenreijs EP, Seyger MMB.   +6 more
europepmc   +1 more source