Results 11 to 20 of about 755 (130)
Ulcère de cornée chronique révélant un syndrome de Parry-Romberg: à propos d´un cas
Le syndrome de Parry-Romberg, est une entité clinique rare, il est caractérisé par une atrophie hémifaciale progressive et associé à diverses manifestations systémiques, notamment ophtalmologiques, neurologiques et maxillo-faciales dont la prise en ...
Sara El Maroufi +4 more
doaj +1 more source
Cell-Assisted Lipotransfer for the Treatment of Parry-Romberg Syndrome [PDF]
Progressive facial hemiatrophy, also known as Parry-Romberg syndrome, is a progressive and self-limited deformation of the subcutaneous tissue volume on one side of the face that creates craniofacial asymmetry.
Yanko Castro-Govea +6 more
doaj +2 more sources
MRI findings of contralateral oculomotor nerve palsy in Parry-Romberg syndrome
Purpose: To study a case of right Parry Romberg syndrome associated with contralateral oculomotor nerve palsy using high-resolution cerebral and orbital magnetic resonance imaging (MRI). Observations: There were no brain MRI abnormalities. However, there
Emily K. Tam +2 more
doaj +1 more source
Role of imaging in morphea assessment: A review of the literature
Abstract Background Localized scleroderma, known as morphea, is a connective tissue disorder characterized by inflammation and fibrosis of the skin and the soft tissue. There exist no universally accepted validated outcome measures in order to monitor the disease activity.
Faezeh Khorasanizadeh +2 more
wiley +1 more source
Scientific opinion on the tolerable upper intake level for vitamin B6
Abstract Following a request from the European Commission, the EFSA Panel on Nutrition, Novel Foods and Food Allergens (NDA) was asked to deliver a scientific opinion on the tolerable upper intake level (UL) for vitamin B6. Systematic reviews of the literature were conducted by a contractor.
EFSA Panel on Nutrition +21 more
wiley +1 more source
Parry-Romberg Syndrome Associated with Localized Scleroderma
Parry-Romberg syndrome is a rare neurocutaneous disorder of unknown origin. It is characterized by progressive facial hemiatrophy and frequently overlaps with a condition known as linear scleroderma ‘en coup de sabre’.
Jelena Maletic +4 more
doaj +1 more source
A Síndrome de Parry-Romberg, também conhecida como atrofia hemifacial progressiva, é uma doença rara caracterizada por lenta e progressiva atrofia de hemiface. O tratamento ofertado para a síndrome, geralmente, visa melhorar o aspecto estético.
Júlio César Garcia de Alencar +3 more
doaj +1 more source
Parry Romberg syndrome: A rare case report
The Parry Romberg syndrome (PRS) is a rare neurocutaneous disorder characterized by progressive facial hemiatrophy. Parry Romberg syndrome is characterized by a slow progressive atrophy that appears in the early stages of life, primarily affecting the ...
Raj Kumar Badam +3 more
doaj +1 more source
Objective: To present a case of progressive hemifacial atrophy in a young woman with Parry-Romberg Syndrome and the role of autologous fat transfer to improve her aesthetic appearance and lessen facial asymmetry.
Ma. Nina Kristine Sison +2 more
doaj +1 more source
Demyelinating etiology as a possible cause of Parry–Romberg Syndrome (PP-14) [PDF]
Parry–Romberg syndrome (PRS) is a rare disease that causes hemiatrophy of the face. The pathophysiological mechanisms involved in its etiology are unknown, but several previous reports suggest the involvement of autoimmune factors.
K. Bahrami +2 more
doaj

