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Parry-Romberg syndrome, which is also known as progressive facial hemiatrophy, is a variant of localized scleroderma. This is a rare condition (OMIM # 141300), characterized by a progressive but self-limited atrophy of the skin and subcutaneous tissue on
Alexis-Virgil Cochino +2 more
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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
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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
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Genetic variations in patient with Parry–Romberg syndrome
Parry–Romberg syndrome is a rare craniofacial disorder which is characterized by progressive facial atrophy. The etiology and pathogenesis of the disease are not known. Herein, we report the genetic variants in patient with this disease.
Bao-Fu Yu +3 more
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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
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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
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Reconstruction of facial hemiatrophy using calcium hydroxylapatite filler: report of a safe and minimally invasive technique [PDF]
Introduction: Progressive Facial Hemiatrophy, also known as Parry Romberg Syndrome, is a rare form of linear scleroderma. The management of facial atrophy sequelae is challenging.
Rossana Cantanhede Farias de Vasconcelos +2 more
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A case of parasympathetic hyperactivity and associated Parry–Romberg syndrome
This case report describes a 46-year-old female with a history of multiple endocrine neoplasia type 1 syndrome status post-parathyroidectomy, thymectomy via robotic video-assisted thoracoscopic surgery, and pituitary adenoma resection presenting with ...
Andrea N Clapp, Anna DePold Hohler
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Parry⁃Romberg syndrome: two cases report and literature review
Objective Parry⁃Romberg syndrome is a rare disease characterized by unilateral facial progressive atrophy accompanied by ipsilateral intracranial lesions and/or cerebral atrophy, this article is aimed to analyze the clinical, radiological and ...
SHA Yu⁃hui +4 more
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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
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