Results 91 to 100 of about 1,771 (170)
UEG Week 2025 Moderated Posters
United European Gastroenterology Journal, Volume 13, Issue S8, Page S189-S802, October 2025.
wiley +1 more source
Oral manifestations of Parry-Romberg syndrome: A review of literature
Parry-Romberg syndrome (PRS) or progressive facial hemiatrophy is a developmental craniofacial disorder of unknown etiology characterized by a slowly progressive unilateral facial atrophy.
Nader A Al-Aizari +4 more
doaj +1 more source
A Case Report of Parry-Romberg Syndrome
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 +3 more
doaj
Síndrome de Parry-Romberg: Visión de su tratamiento Parry-Romberg's syndrome: View of its treatment
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 +4 more
doaj
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 +3 more
doaj +1 more source
Progressive hemifacial atrophy : Case report [PDF]
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 atrophy affecting one side of the face. The incidence and the cause of this
Camarinha-da Silva, Camila +5 more
core
Late-onset Parry–Romberg syndrome in a patient with newly diagnosed HIV-2 infection
Sclerodermoid syndromes encompass a wide spectrum of rare diseases, with variable clinical presentation and severity. We present a case of a 31-year-old woman, Fitzpatrick’s phototype V, who presented to our dermatology department with a 5-year history ...
Claúdia Brazão +7 more
doaj
Identification of the molecular basis of the lacrimo-auriculo-dento-digital (LADD) syndrome [PDF]
Lacrimo-auriculo-dento-digital (LADD) syndrome, also known as Levy-Hollister syndrome, is a rare autosomal dominant developmental disorder, mainly characterized by abnormalities of the lacrimal system and salivary glands, ears and hearing, teeth and ...
Rohmann, Edyta
core
Parry Romberg Syndrome: A Case Report and an Insight Into Etiology. [PDF]
Kumar M +4 more
europepmc +1 more source

