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Coexistence of Localized and Systemic Juvenile Scleroderma: A Case Report and Review of Literature. [PDF]
Clin Case RepABSTRACT Juvenile scleroderma (JS) is a rare chronic connective tissue disorder characterized by progressive fibrosis of the skin and soft tissues with/without internal organ involvements. Scleroderma manifests itself in both systemic (SSc) and localized (LS) forms.
Miremarati A +4 more
europepmc +2 more sources
Romanian Journal of Rheumatology, 2016 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
doaj +1 more source
Parry-Romberg Syndrome: A Case of Late Onset with Rapid Progression [PDF]
Journal of Clinical and Diagnostic Research, 2014 Parry–Romberg syndrome (PRS) or progressive hemifacial atrophy is rare, poorly understood condition with an unclear aetiology and characterized by slow and progressive atrophy affecting one side of the face.
Senthil Kumar +4 more
doaj +1 more source
Journal of Medical Case Reports, 2019 Background Parry–Romberg syndrome, also known as progressive hemifacial atrophy, is a rare degenerative disorder with numerous distinctive clinical presentations. It is usually slowly progressive, occurring more in females, and affects primarily one side
Jimmy Girgis William Abdelnour +3 more
doaj +1 more source
Clinical Neurophysiology Practice, 2021 Objective: Hemifacial atrophy (HFA) is a rare disorder characterized by progressive unilateral wasting facial soft tissue, muscle, and/or bone. Trigeminal nerve abnormalities may contribute to or result from disease pathophysiology.
Michael P. Skolka +4 more
doaj +1 more source
A unique case of progressive hemifacial microsomia or Parry-Romberg syndrome associated with limb and brain anomalies with normal neurological findings: A review of the literature [PDF]
, 2021 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 ...
Sabeti, Sara +6 more
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Progressive Hemifacial Atrophy After Implant Placement in Patients Taking Immunosuppressive Agents [PDF]
, 2019 Progressive hemifacial atrophy (PHA) is a rare disorder characterized by acquired unilateral facial atrophy. This disease mainly affects the skin and the craniofacial tissue below forehead. It also involves dermatomes of the fifth cranial nerve.
김학진 +3 more
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Parry⁃Romberg syndrome: two cases report and literature review
Chinese Journal of Contemporary Neurology and Neurosurgery, 2023 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
doaj +1 more source
, 2013 We report the case of a 44-year-old woman with a one-year history of en coup de sabre morphea and progressive hemifacial atrophy with ipsilateral hemifacial neuralgia, migraine, and contralateral neurologic abnormalities.
Vedvyas, Chetan, Urbanek, Richard W
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