Results 31 to 40 of about 755 (130)
Parry-Romberg Syndrome: a Rare Case Report
eJournal of Oral Maxillofacial Research, 2011 Background: The purpose of this report is to present a rare entity of Parry-Romberg syndrome. This poorly understood degenerative condition is characterised by atrophic changes affecting one side of the face.
Anusha Laxman Rangare +3 more
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Clinical Case Reports, Volume 13, Issue 4, April 2025.ABSTRACT The present investigation aimed to inform the radiologists about the imaging features of injectable fillers in order not to confound these with true pathology or vice versa in order not to miss true pathology obscured by filler injections.
Gloria Bettini +4 more
wiley +1 more source
Você conhece esta síndrome? Do you know this syndrome?
Anais Brasileiros de Dermatologia, 2007 Trata-se de criança de oito anos, portadora de atrofia na hemiface direita, desde os seis anos. A ressonância magnética do encéfalo evidenciou espessamento cortical e formação de cistos.
Luciana Baptista Pereira +3 more
doaj +1 more source
Progressive facial deformity from childhood to adulthood in a patient of Parry-Romberg syndrome
Journal of Cleft Lip Palate and Craniofacial Anomalies, 2020 Parry-Romberg syndrome (PRS) is an uncommon degenerative craniofacial condition characterized by a slow, progressive, and unilateral atrophy of facial tissues, including muscles, cartilage, nerves, bones, and skin.
Neeraj Yadav +3 more
doaj +1 more source
Augmented Reality Navigation in Craniomaxillofacial/Head and Neck Surgery
OTO Open, Volume 9, Issue 2, April-June 2025.Abstract Objective This study aims to (1) develop an augmented reality (AR) navigation platform for craniomaxillofacial (CMF) and head and neck surgery; (2) apply it to a range of surgical cases; and (3) evaluate the advantages, disadvantages, and clinical opportunities for AR navigation. Study Design A multi‐center retrospective case series.
E. Brandon Strong +18 more
wiley +1 more source
Comparison of 3D facial photographs and clinical documentation in patients with craniofacial morphea
Skin Health and Disease, Volume 4, Issue 6, December 2024.Craniofacial morphea (CM) is a rare autoimmune disease characterised by progressive atrophy of the skin and soft tissue of the face, resulting in facial asymmetry. With the involvement of varying practices in the care of patients with CM, consistent documentation of disease location and severity lack standardized evaluation.
Tyler T. Nguyen +5 more
wiley +1 more source
Case report of progressive facial hemiatrophy
Journal of Holistic Nursing and Midwifery, 2007 Introduction: Progressive facial hemiatrophy (Parry-Romberg syndrome) is a rare disease always with neurological symptoms such as migraine and epilepsy.
tahereh seyednoori +2 more
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Discrepancy between IDSA and ESGBOR in Lyme disease: Individual participant meta‐analysis in Türkiye
Zoonoses and Public Health, Volume 71, Issue 4, Page 337-348, June 2024.Abstract Background The evidence on the prevalence of Lyme borreliosis (LB) is limited, but there is a suspicion of overdiagnosis of LB in recent years. We reviewed the LB diagnosis and treatment‐related data in Türkiye, based on the Infectious Diseases Society of America (IDSA) 2020 and European Society of Clinical Microbiology and Infectious Diseases
Abdullah Burak Yıldız +5 more
wiley +1 more source
BMC Neurology, 2009 Background Hemifacial atrophy (Parry-Romberg syndrome) is a relatively rare disease. The etiology of the disease is not clear. Some authors postulate its relation with limited scleroderma linearis.
Brzezińska-Wcisło Ligia +2 more
doaj +1 more source
Revista Ciencias Biomédicas, 2015 Introduction: the progressive hemifacial atrophy or Parry-Romberg syndrome is a rare disease, of slow clinical evolution that generates atrophy of the soft tissues.
Redondo-Bermúdez César +4 more
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