Results 81 to 90 of about 1,924 (163)

Progressive hemifacial atrophy

Dental Research Journal, 2013
Progressive hemifacial atrophy, also known as Parry-Romberg Syndrome, is an uncommon degenerative and poorly understood condition. It is characterized by a slow and progressive but self-limited atrophy affecting one side of the face.
Abhijeet Sande, Mukund Risbud, Avinash Kshar, Arati Oka Paranjpe   +3 more
doaj   +1 more source

Minimally Invasive Combined Treatment for Parry-Romberg Syndrome

, 2009
BACKGROUND: Facial hemiatrophy, a typical manifestation of Parry-Romberg syndrome, produces massive face asymmetry, causing marked aesthetic damage and severe psychological discomfort, with repercussions to the psychophysical status of the patient.
RIZZO MI, Marco Mazzocchi, ONESTI MG, SCUDERI N., ONESTI, Maria Giuseppina, RIZZO, MARIA IDA, MONARCA C, MONARCA, Cristiano, MAZZOCCHI, Marco, SCUDERI, Nicolo'   +9 more
core   +1 more source

UEG Week 2025 Moderated Posters

United European Gastroenterology Journal, Volume 13, Issue S8, Page S189-S802, October 2025.
wiley   +1 more source

A rare case of Parry-Romberg syndrome with restrictive strabismus

Indian Journal of Ophthalmology. Case Reports
Parry-Romberg syndrome is a rare disease characterized by slowly progressive atrophy affecting facial subcutaneous tissues, muscles, osteocartilaginous structures, and possible cerebral involvement.
Nikita Sah, Damaris Magdalene, Ganesh Kuri, Harsha Bhattacharjee, Swanubhuti Jain   +4 more
doaj   +1 more source

A Case Report of Parry-Romberg Syndrome

پزشکی بالینی ابن سینا, 2017
Introduction: Parry-Romberg syndrome, a rare syndrome, is characterized by progressive atrophy affecting one side of the face. This disease can include the skin, subcutaneous tissue, muscles, cartilage, and underlying bony structures. Case Presentation:
P Alirezaei, L Khezrian, H Ghasemi Basir, S Khanali   +3 more
doaj  

Síndrome de Parry-Romberg: Visión de su tratamiento Parry-Romberg's syndrome: View of its treatment

Revista Cubana de Estomatología, 2005
El síndrome de Parry-Romberg o atrofia hemifacial progresiva, enfermedad de Romberg o también denominada trofoneurosis facial, fue descrito por Parry en 1925 y por Romberg en 1946.
María Elena González Espíndola, Yulenia Cruz Rivas, Brismayda García González, Librado Vergara Piedra1, Libia Mena García   +4 more
doaj  

A Hybrid Technique Using Video Laryngoscope-assisted Flexible Bronchoscopy to Facilitate Endotracheal Intubation in Children with Anticipated Difficult Airway: A Case Series

Turkish Journal of Anaesthesiology and Reanimation
We present a case series using a hybrid technique of video laryngoscope-assisted flexible bronchoscopy to facilitate endotracheal intubation in children with anticipated difficult airway.
K. Gunasekaran, Reesha Joshi, Pradeep Karunagaran, V.S.G. Yachendra   +3 more
doaj   +1 more source

Síndrome de Parry-Romberg: hemiatrofia facial progresiva. Reporte de Caso.: Síndrome de Parry-Romberg.

, 2020
Introduction: Parry-Romberg Syndrome is a neurocutaneous disorder, very rare and characterized by progressive facial hemiatrophy, the first clinical sign is facial asymmetry. SPR occurs simultaneously with high frequency with linear scleroderma.
Mejía Escobar, Cinthya Karina, Sánchez Sierra, Luis Enrique, Salgado, Ana Luisa   +2 more
core  

ASPECTOS CLÍNICOS DA SÍNDROME DE PARRY-ROMBERG: RELATO DE CASO

, 2014
Introduction: progressive hemifacial atrophy, also known as Parry-Romberg syndrome, is a rare degenerative disease, etiology unclear. Is characterized by a slow and progressive atrophy that affects the face unilaterally.
Cheffer, Leticia Almeida, de Azevedo, Roberto Almeida, Malaquias, Pietry Dy Tarso Inã Alves, Figueiredo, Leonardo Morais Godoy, Vasconcelos Oliveira, Gabriel Queiroz, Macêdo, Thiago Felippe Oliveira   +5 more
core   +1 more source

Parry-Romberg syndrome studied by optical coherence tomography

, 2008
A case of Parry-Romberg syndrome that was studied by fluorescein angiography and optical coherence tomography (OCT) is described. OCT revealed the existence of retinal nerve fiber layer edema and abnormalities of the vitreoretinal interface. The presence
Theodossiadis, G.P., Emfietzoglou, I., Grigoropoulos, V.G., Theodossiadis, P.G., Papaspirou, A., Vergados, I., Nikolaidis, P.   +6 more
core