Results 1 to 10 of about 772 (152)
A case report of Parry–Romberg syndrome [PDF]
Clinical Case ReportsKey Clinical Message Parry–Romberg syndrome is characterized by progressive dystrophy in one half of the face, which usually begins in childhood. Correct and timely diagnosis of this disease, as well as a multidisciplinary approach and timely surgical ...
Kiana Babaei +3 more
doaj +5 more sources
Romanian Journal of Rheumatology, 2016 Parry-Romberg syndrome, which is also known as progressive facial hemiatrophy, is a variant of localized scleroderma. This is a rare condition (OMIM # 141300), characterized by a progressive but self-limited atrophy of the skin and subcutaneous tissue on
Alexis-Virgil Cochino +2 more
doaj +5 more sources
Genetic variations in patient with Parry–Romberg syndrome [PDF]
Scientific Reports, 2023 Parry–Romberg syndrome is a rare craniofacial disorder which is characterized by progressive facial atrophy. The etiology and pathogenesis of the disease are not known. Herein, we report the genetic variants in patient with this disease.
Bao-Fu Yu +3 more
doaj +2 more sources
A case of parasympathetic hyperactivity and associated Parry–Romberg syndrome [PDF]
SAGE Open Medical Case Reports, 2021 This case report describes a 46-year-old female with a history of multiple endocrine neoplasia type 1 syndrome status post-parathyroidectomy, thymectomy via robotic video-assisted thoracoscopic surgery, and pituitary adenoma resection presenting with ...
Andrea N Clapp, Anna DePold Hohler
doaj +2 more sources
Clinics in Plastic Surgery, 2019 Parry-Romberg syndrome, or progressive hemifacial atrophy, is a rare disorder of unknown etiology. Patients present with unilateral atrophy of skin that may progress to involve underlying fat, muscle, and osseocartilaginous structures. Neurologic complications are common.
Renata Maricevich +2 more
exaly +4 more sources
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
doaj +3 more sources
Lens subluxation combined with parry-romberg syndrome: case report [PDF]
BMC OphthalmologyBackground Parry-Romberg syndrome (PRS) is a rare progressive degenerative disorder of unknown etiology. Here we report a rare case of PRS combined with lens subluxation in Eye and ENT hospital of Fudan University, Shanghai.
Yating Tang +3 more
doaj +2 more sources
Parry Romberg syndrome: A case report. [PDF]
Radiol Case RepParry Romberg syndrome (PRS) is a rare self-limiting disease, typically occurring in children and young adults, that causes slow progressive atrophy of one-half of the face. It primarily affects the subcutaneous tissue and skin with some cases exhibiting deeper extension to glandular, osseous and muscular structures.
Afreh YA +5 more
europepmc +3 more sources
Parry-romberg syndrome: about a case
The Pan African Medical Journal, 2017 A six-year-old girl presented with skin lesions on the left cheek at 5 years of age. On examination diffuse sclerosis on the left cheek was noted, hypoplasia of left half of the face and deviation of mouth and lips to left side were noted. Investigations
Hanane Oummad, Lalla Ouafae Cherkaoui
doaj +3 more sources
Journal of Dermatological Case Reports, 2010 Parry-Romberg syndrome (PRS) or idiopathic hemifacial atrophy is a rare neurocutaneous syndrome. It is characterized by slowly progressive atrophy, located on one side of the face, primarily involving the skin, fat and connective tissue. PRS seems to overlap with "en coupe de sabre" morphea.We present a case of hemifacial atrophy in a 14-year-old boy ...
Elizabeth, Lazaridou +5 more
+8 more sources