Results 21 to 30 of about 1,924 (163)
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
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
Coexistence of Parry-Romberg syndrome with homolateral segmental vitiligo [PDF]
Parry-Romberg syndrome or progressive facial hemiatrophy was first described by Caleb Parry in 1825 and Moritz Romberg in 1846. This disorder is characterized by slowly progressing acquired unilateral hemifacial atrophy, which affects subcutaneous ...
Janowska, Marta +3 more
core +1 more source
Clinical evolution of neuroretinitis in Parry-Romberg syndrome
A 16-year-old girl with Parry-Romberg syndrome presented with monolateral exudative neuroretinitis and retinal telangiectasis that had been observed for 42 months. She was treated with immunosuppressive therapy with A-cyclosporine for I year, followed by
Giuseppe de Crecchio +9 more
core +3 more sources
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
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
Orofacial myofunctional characterization in Parry-Romberg syndrome [PDF]
Objetivo: Caracterizar os aspectos miofuncionais orofaciais de pacientes acometidos pela síndrome de Parry-Romberg, por meio de protocolos clínicos padronizados e da Eletromiografia de Superfície (EMGs) dos músculos mastigatórios.
Sassi, Fernanda Chiarion +3 more
core +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
Parry Romberg Syndrome. An unusual case with dental features.
Parry-Romberg syndrome, also known as progressive hemi facial atrophy has been described as having clinical overlap with Morphea en coup de sabre or linear scleroderma.
Cj Bates, Hamed Safaei*, Tk Mittal
core +1 more source

