Results 41 to 50 of about 1,924 (163)

Sklerosierende Erkrankungen der Haut

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 10, Page 1282-1303, October 2025.
Zusammenfassung Sklerosierende Hautkrankheiten sind eine Gruppe unterschiedlicher dermatologischer Erkrankungen, die durch fibrotische Veränderungen gekennzeichnet sind und die Lebensqualität der Patienten stark einschränken können. Diese Erkrankungen treten häufig mit kutanen Manifestationen auf und können in bestimmten Fällen auch extrakutanes Gewebe
Yasamin Kalantari   +4 more
wiley   +1 more source

Increasing Incidence of Facial Nerve Disorders in the United States from 2007 to 2022

open access: yesThe Laryngoscope, Volume 135, Issue 6, Page 2008-2013, June 2025.
In this study of national administrative claims data from 2007 to 2022, the mean annual incidence of facial nerve disorders was 30.5 cases per 100,000 adults. The mean annual incidence of Bell's palsy alone was found to be 24.5/100,000, with increasing annual incidence rates during the study period.
Eric X. Wei   +3 more
wiley   +1 more source

Lipostructure in Parry-Romberg Disease

open access: yes, 2012
Parry-Romberg syndrome is a disease characterized by progressive hemifacial atrophy. Multiple surgical procedures have been used to improve the facial volume and contours of patients with this disease, including alloplastic, silicone, or collagen ...
TERENZI, VALENTINA   +5 more
core   +1 more source

Sequential MRI as a Diagnostic Tool for Follow‐Up of Hyaluronic Acid Dermal Filler, in a Woman Who Underwent Radiation Therapy for Oral Cancer

open access: yesClinical Case Reports, Volume 13, Issue 4, April 2025.
ABSTRACT The present investigation aimed to inform the radiologists about the imaging features of injectable fillers in order not to confound these with true pathology or vice versa in order not to miss true pathology obscured by filler injections.
Gloria Bettini   +4 more
wiley   +1 more source

Você conhece esta síndrome? Do you know this syndrome?

open access: yesAnais 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   +3 more
doaj   +1 more source

Progressive facial deformity from childhood to adulthood in a patient of Parry-Romberg syndrome

open access: yesJournal 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   +3 more
doaj   +1 more source

Case report of progressive facial hemiatrophy

open access: yesJournal of Holistic Nursing and Midwifery, 2007
Introduction: Progressive facial hemiatrophy (Parry-Romberg syndrome) is a rare disease ‎always with neurological symptoms such as migraine and epilepsy.
tahereh seyednoori   +2 more
doaj  

Augmented Reality Navigation in Craniomaxillofacial/Head and Neck Surgery

open access: yesOTO Open, Volume 9, Issue 2, April-June 2025.
Abstract Objective This study aims to (1) develop an augmented reality (AR) navigation platform for craniomaxillofacial (CMF) and head and neck surgery; (2) apply it to a range of surgical cases; and (3) evaluate the advantages, disadvantages, and clinical opportunities for AR navigation. Study Design A multi‐center retrospective case series.
E. Brandon Strong   +18 more
wiley   +1 more source

Parry-Romberg Syndrome with Intracranial Vascular Dysplasia: A case report [PDF]

open access: yes, 2002
Parry-Romberg syndrome is characterized by slowly progressive but self-limited atrophy of the facial subcutaneous fat, which can be followed by wasting of associated skin, cartilage, connective or ocular tissue, muscle and bone.
신지철, 박창일
core  

Parry-Romberg syndrome in a pediatric patient. A case report.

open access: yes, 2015
The Parry-Romberg syndrome is a rare degenerative disease of unknown etiology that has dental implications. It is characterized by a progressive hemifacial atrophy that appears in the early stages of life.
Lizzete Díaz, Carmen Ayala, Edgar Reyes
core   +2 more sources

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