Results 31 to 40 of about 133 (87)

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, Rodrigo Santiago Gómez, Cláudia Márcia Resende Silva, Wandilza Fátima dos Santos   +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, Deepak Kumar Gupta, Ashok Utreja, Arun Kumar Garg   +3 more
doaj   +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, Stephanie M. Cohen, Katharina S. Shaw, Fatma Dedeoglu, Ruth Ann Vleugels, Ingrid M. Ganske   +5 more
wiley   +1 more source

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, Ecesu Çetin, Fatihan Pınarlık, Şiran Keske, Füsun Can, Önder Ergönül   +5 more
wiley   +1 more source

PARRY-ROMBERG SYNDROME

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, Redondo-De Oro Katherine, Mendoza-Suárez Liney, Barrios-Barreto Rina, Buj-Vargas Julián   +4 more
doaj  

"Scleroderma linearis: hemiatrophia faciei progressiva (Parry-Romberg syndrom) without any changes in CNS and linear scleroderma "en coup de sabre" with CNS tumor

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, Lis-Święty Anna, Bergler-Czop Beata   +2 more
doaj   +1 more source

Progressive hemifacial atrophy Parry Romberg syndrome characteristics of craniofacial morphology [PDF]

Stomatološki glasnik Srbije, 2007
The aim of this case report was to analyze clinical finding in a patient with rare, Parry Romberg syndrome. The patient was diagnosed with progressive facial hemiatrophy that affected skin, subcutaneous tissue and underlying bony structures.
Nikodijević-Latinović Angelina
doaj   +1 more source

Neurological, cardiac, musculoskeletal, and renal manifestations of scleroderma along with insights into its genetics, pathophysiology, diagnostic, and therapeutic updates

Health Science Reports, Volume 7, Issue 4, April 2024.
Abstract Background Scleroderma, also referred to as systemic sclerosis, is a multifaceted autoimmune condition characterized by abnormal fibrosis and impaired vascular function. Pathologically, it encompasses the persistent presence of inflammation, abnormal collagen buildup, and restructuring of blood vessels in various organs, resulting in a wide ...
Priyadarshi Prajjwal, Mohammed Dheyaa Marsool Marsool, Vikas Yadav, Ramya S. D. Kanagala, Yeruva Bheemeswara Reddy, Jobby John, Justin Riley Lam, Nanditha Karra, Bita Amiri, Moiz Ul Islam, Venkatesh Nithya, Ali Dheyaa Marsool Marsool, Srikanth Gadam, Neel Vora, Omniat Amir Hussin   +14 more
wiley   +1 more source

Chronologic Presentation of a Severe Case of Progressive Hemifacial Atrophy (Parry-Romberg Syndrome) with the Loss of an Eye

Case Reports in Otolaryngology, 2014
Progressive hemifacial atrophy, also known as Parry-Romberg syndrome, is a slowly advancing degenerative disease that mostly affects the cutaneous, subcutaneous fatty tissue, muscle tissue, and bone structures on one side of the face.
Mesut Kaya, Ceyda Sel Yilmaz, Hanifi Kurtaran, Mehmet Gunduz   +3 more
doaj   +1 more source

S2k guideline: Diagnosis and therapy of localized scleroderma

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 4, Page 605-620, April 2024.
Summary The updated S2k guideline deals with the diagnosis and therapy of localized scleroderma (LoS). LoS represents a spectrum of sclerotic skin diseases in which, depending on the subtype and localisation, structures such as adipose tissue, muscles, joints, and bones may also be affected.
Alexander Kreuter, Pia Moinzadeh, Maria Kinberger, Gerd Horneff, Margitta Worm, Ricardo N. Werner, Andreas Hammacher, Thomas Krieg, Jörg Wenzel, Michael Oeschger, Lisa Weibel, Robert Müllegger, Nicolas Hunzelmann   +12 more
wiley   +1 more source