Results 51 to 60 of about 1,281,448 (141)

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 with localized scleroderma: a case report [PDF]

, 2014
Parry Romberg syndrome(PRS) is a rare acquired poorly understood neurocutaneous syndrome of unknown etiology characterized by slow progressive atrophic changes commonly affecting one half of the face. The exact incidence and etiology towards the syndrome
Gupta, Nikita, Negi, Raju, Khan, Mubeen, Khan, Mohsin   +3 more
core  

Parry Romberg Syndrome: 7 Cases and Literature Review

, 2015
Parry Romberg syndrome is a rare progressive hemiatrophy of the face that typically occurs in children and young adults and has a peculiar progression that ceases without apparent cause after a highly variable period. Only a subset of patients with Parry
Hagiwara, M., Wong, M., Shatzkes, D. R., Phillips, C. D.   +3 more
core   +1 more source

Orofacial myofunctional characterization in Parry-Romberg syndrome [PDF]

, 2015
Objetivo: Caracterizar os aspectos miofuncionais orofaciais de pacientes acometidos pela síndrome de Parry-Romberg, por meio de protocolos clínicos padronizados e da Eletromiografia de Superfície (EMGs) dos músculos mastigatórios.
Sassi, Fernanda Chiarion, Rocha, Bruna Rainho, Andrade, Claudia Regina Furquim de, Mangilli, Laura Davison   +3 more
core   +1 more source

"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

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

Difficult mask ventilation made easy: Three cases of Parry Romberg syndrome

Indian Journal of Anaesthesia, 2016
Parry Romberg syndrome presenting as hemifacial atrophy poses various perioperative problems due to multi-system involvement. These patients have several anaesthetic implications which are published as case reports.
Kavitha Jayaram, Indira Gurajala, Gopinath Ramachandran   +2 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

Parry–Romberg syndrome associated with en coup de sabre in a patient from South Sudan – a rare entity from East Africa: a case report

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, Youeil Girgis William Abdelnour, Rose-Mery Amin Boushra Kerollos, Ziryab Imad Taha Mahmoud   +3 more
doaj   +1 more source

S2k‐Leitlinie: Diagnostik und Therapie der zirkumskripten Sklerodermie

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 4, Page 605-621, April 2024.
Zusammenfassung Die vorliegende aktualisierte S2k‐Leitlinie befasst sich mit der Diagnostik und der Therapie der zirkumskripten Sklerodermie (ZS). Diese umfasst ein Spektrum sklerotischer Erkrankungen der Haut mit, je nach Subtyp und Lokalisation, möglicher Beteiligung von hautnahen Strukturen wie Fettgewebe, Muskulatur, Gelenke und Knochen. Ein Befall
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