Results 11 to 20 of about 133 (87)
Clinical Anatomy, Volume 36, Issue 3, Page 503-526, April 2023., 2023 Abstract The ever‐increasing scope of physiotherapy practice is raising questions on what anatomical knowledge and skills ought to be taught within qualifying physiotherapy degree programmes in the United Kingdom (UK). The aim of the study was to create core anatomical knowledge and skills learning objectives to inform knowledge and skills for entry ...
Hope Gangata +3 more
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Parry-Romberg Syndrome Associated with Localized Scleroderma
Case Reports in Neurology, 2010 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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Parry-Romberg syndrome in a pediatric patient. A case report.
Journal of Oral Research, 2015 The Parry-Romberg syndrome is a rare degenerative disease of unknown etiology that has dental implications. It is characterized by a progressive hemifacial atrophy that appears in the early stages of life.
Edgar Reyes, Carmen Ayala, Lizzete Díaz
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Anais Brasileiros de Dermatologia, 2011 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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Philippine Journal of Otolaryngology Head and Neck Surgery, 2019 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
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Parry Romberg syndrome: A rare case report
Journal of Indian Academy of Oral Medicine and Radiology, 2014 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
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Demyelinating etiology as a possible cause of Parry–Romberg Syndrome (PP-14) [PDF]
Neurology Letters, 2023 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
Dyke‐Davidoff‐Masson Syndrome: A Case of Unilateral Cerebral Atrophy and Seizure Disorder
Clinical Case Reports, Volume 14, Issue 2, February 2026.ABSTRACT Dyke‐Davidoff‐Masson syndrome (DDMS) is an infrequently occurring neurological entity characterized by cerebral hemiatrophy and a collection of cognitive, motor and seizure‐related symptoms. We describe the case of an 18‐year‐old male with a long‐standing history of generalized tonic–clonic seizures following a significant fall at the age of 4.
Wasfa Shafiq +7 more
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Coexistence of Localized and Systemic Juvenile Scleroderma: A Case Report and Review of Literature
Clinical Case Reports, Volume 13, Issue 10, October 2025.ABSTRACT 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.
Aye Miremarati +4 more
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Unveiling Parry-Romberg Syndrome With Native Demyelinating Etiology as the Underlying Cause
Acta Medica IranicaParry-Romberg Syndrome (PRS) is an atypical condition characterized by hemiatrophy of the face. Despite its rarity, the precise pathophysiological processes underlying its etiology remain elusive.
Kaveh Bahram +4 more
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