Introduction to Romberg Syndrome

What is/are Romberg Syndrome?

Romberg Syndrome - Recently, it has been applied to correct localized tissue atrophy, burns, hemifacial atrophy (Parry-Romberg syndrome, scleroderma, anophthalmic orbit), and loss of substance resulting from trauma, tumor excision, and congenital craniofacial deformity sequelae. ^[1] 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 parasympathetic hyperactivity and Parry–Romberg syndrome. ^[2] Prior trauma (congenital depression, leptomeningeal cysts, posttraumatic osteolysis), surgical intervention (flap osteonecrosis and burr holes), infection, and inflammatory processes (sarcoidosis) can result in focal bone loss, which may also be seen with idiopathic disorders without (bilateral parietal thinning and Gorham disease) or with (Parry-Romberg syndrome) atrophy of the overlying soft tissues. ^[3] This work aims to present a case of retinal vasculitis associated with Parry-Romberg syndrome. ^[4] Highlights • Progressive haemifacial atrophy, also known as Parry-Romberg syndrome. ^[5] Parry-Romberg syndrome (PRS) is a rare condition that causes progressive but selflimited atrophy of facial tissues, muscles, and osteocartilaginous and cerebral structures. ^[6] Age, Parry-Romberg syndrome, previous facial bone surgery at the site that received fat grafting, and injected volume were independently negative (all p < 0. ^[7] Methods A prospective analysis was conducted of skeletally immature patients (n = 73) with craniofacial microsomia and Parry-Romberg syndrome who underwent isolated fat grafting (with no previous or concomitant bone surgery) using anatomical surgical principles (facial subunits and fat compartments) for the reconstruction of lower face volumetric asymmetry. ^[8] Parry-Romberg syndrome (PRS) is a progressive facial hemiatrophy often associated with severe epilepsy. ^[9] 05) superior to initial retention rates for patients aged 18 years or older, those with Parry-Romberg syndrome, those who had undergone previous craniofacial bone surgery, and those with a recipient site at the forehead unit. ^[10] Progressive facial hemiatrophy or Parry–Romberg syndrome is a rare disorder of unknown etiology which is characterized by atrophy of the one side of the face and various neurological complications. ^[11] This is a rare case of linear scleroderma and Parry–Romberg syndrome presenting with widespread ipsilateral neurogenic manifestations. ^[12] Parry‐Romberg syndrome is a hemifacial atrophy which can be complicated by melasma. ^[13] Parry‐Romberg syndrome (PRS) is characterized by hemiatrophy of facial structures, including skin, subcutaneous fat, muscle, bone, and cartilage. ^[14] Autologous free fat graft is a widely accepted method of facial contour restoration in Parry-Romberg syndrome (PRS); however, complex and unpredictable facial anatomy can render this surgery extremely challenging. ^[15] Purpose: We describe a case of Parry-Romberg syndrome (PRS) presenting with panuveitis and retinal vasculitis. ^[16] ABSTRACT The authors describe a patient with Parry–Romberg syndrome (PRS) who had acquired monocular elevation deficit (MED), ptosis, and facial hemiatrophy. ^[17] Parry-Romberg syndrome was negatively associated (P < 0. ^[18] The Parry-Romberg syndrome (PRS), also known as hemifacial atrophy, is a rare neurocutaneous disease with the prevalence of 1/700,000 cases. ^[19] Parry‐Romberg syndrome is a rare acquired neurocutaneous disorder typically characterized by hemifacial atrophy. ^[20] Results: Circumscribed morphea was the most common subtype (34, 42%) of the 81 patients, followed by linear morphea (21, 26%), generalized morphea (14, 17%), en coup de sabre (11, 14%) and Parry–Romberg syndrome (1, 1%). ^[21] Parry‐Romberg syndrome (PRS) is a rare condition involving self‐limited progressive facial hemiatrophy. ^[22]

progressive hemifacial atrophy

Dear editor, Parry Romberg syndrome (PRS), also known as progressive hemifacial atrophy, is a rare craniofacial disorder characterized by unilateral facial atrophy affecting the skin, subcutis, muscle, and bones. ^[1] Parry Romberg syndrome (PRS), also called progressive hemifacial atrophy (PHF), is a rare, mostly sporadic, syndrome of unknown etiology characterized by a progressive self-limited but irreversible atrophy on one side of the face and sometimes the ipsilateral trunk and limbs [1]. ^[2] Parry-Romberg syndrome (PRS) is a rare condition characterized by slow and progressive hemifacial atrophy [1]. ^[3] Parry-Romberg syndrome (PRS) is a rare facial deformity characterised by slowly progressive hemifacial atrophy. ^[4] BACKGROUND Parry-Romberg syndrome is a neuro-cutaneous disease characterized by progressive hemifacial atrophy. ^[5] In this report, we describe an unusual case of progressive hemifacial atrophy or Parry-Romberg syndrome in a 10-year-old girl with progressive hemifacial microsomia and limb anomalies who had brain magnetic resonance imaging (MRI) findings of white matter hyper-intensities. ^[6] PURPOSE To report three cases of Parry-Romberg syndrome (PRS) with progressive hemifacial atrophy and similar fundus changes. ^[7] BackgroundParry–Romberg syndrome, also known as progressive hemifacial atrophy, is a rare degenerative disorder with numerous distinctive clinical presentations. ^[8] 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. ^[9] Parry-Romberg syndrome, also known as progressive hemifacial atrophy (PHA), is a rare disorder of unknown etiology characterized by unilateral facial atrophy and is associated with multiple ophthalmologic and neurologic manifestations. ^[10] Parry-Romberg Syndrome (PRS), or progressive hemifacial atrophy, is an uncommon disorder characterized by progressive unilateral loss of adipose tissue and underlying structures including muscle, cartilage, and bone, often with little or no sclerosis. ^[11] PURPOSE Parry Romberg syndrome (PRS) is a condition characterized by progressive hemifacial atrophy, predominantly affecting the soft tissues. ^[12] PParry–Romberg syndrome, also known as progressive hemifacial atrophy, is a rare clinical entity of unknown origin with atrophy of skin and subcutaneous fat changes. ^[13] Parry Romberg Syndrome (PRS) - also known as Progressive Hemifacial Atrophy- is a rare disorder primarily affecting the soft tissues on one side of the scalp and face, existing on a spectrum with linear scleroderma and ‘en coup de sabre’ morphoea. ^[14] Parry-Romberg syndrome, or progressive hemifacial atrophy, is a rare disorder of unknown etiology. ^[15] Parry-Romberg syndrome is a rare disorder with progressive hemifacial atrophy of unknown etiology. ^[16] Parry Romberg syndrome (PRS) is an unusual neurological entity characterized by progressive hemifacial atrophy. ^[17]

en coup de

Parry-Romberg syndrome (PRS) and linear sclerosis en coup de sabre (LScs) are rare, related, autoimmune conditions of focal atrophy and sclerosis of head and face which are associated with the development of focal epilepsy. ^[1] Background The aim of this study was to: (i) describe the abnormalities seen on brain imaging in a group of children with en coup de sabre (EDCS) with/without Parry-Romberg syndrome (PRS); and (ii) identify clinical predictors of brain imaging abnormalities. ^[2]

Parry Romberg Syndrome

Dear editor, Parry Romberg syndrome (PRS), also known as progressive hemifacial atrophy, is a rare craniofacial disorder characterized by unilateral facial atrophy affecting the skin, subcutis, muscle, and bones. ^[1] Parry Romberg syndrome (PRS), also called progressive hemifacial atrophy (PHF), is a rare, mostly sporadic, syndrome of unknown etiology characterized by a progressive self-limited but irreversible atrophy on one side of the face and sometimes the ipsilateral trunk and limbs [1]. ^[2] Introduction: The Parry Romberg syndrome (PRS) is a mosaic disease of unknown aetiology which mostly affects women. ^[3] PURPOSE Parry Romberg syndrome (PRS) is a condition characterized by progressive hemifacial atrophy, predominantly affecting the soft tissues. ^[4] Parry Romberg Syndrome (PRS) - also known as Progressive Hemifacial Atrophy- is a rare disorder primarily affecting the soft tissues on one side of the scalp and face, existing on a spectrum with linear scleroderma and ‘en coup de sabre’ morphoea. ^[5] Parry Romberg syndrome (PRS) is also a very rare disease, and the underlying aetiology remains unknown. ^[6] The clinicopathologic and neuroimaging features of the following topics are reviewed in this chapter: bacterial, viral, and fungal infections, histiocytic disorders, rheumatoid arthritis, sarcoidosis, systemic lupus erythematosus, Sjogren syndrome, scleroderma, immunoglobin G4-related disease, Kimura disease, benign osteoma cutis, and Parry Romberg syndrome. ^[7] Parry Romberg syndrome (PRS) is an unusual neurological entity characterized by progressive hemifacial atrophy. ^[8]