Results 31 to 40 of about 772 (152)

Dyke‐Davidoff‐Masson Syndrome: A Case of Unilateral Cerebral Atrophy and Seizure Disorder

open access: yesClinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Dyke‐Davidoff‐Masson syndrome (DDMS) is an infrequently occurring neurological entity characterized by cerebral hemiatrophy and a collection of cognitive, motor and seizure‐related symptoms. We describe the case of an 18‐year‐old male with a long‐standing history of generalized tonic–clonic seizures following a significant fall at the age of 4.
Wasfa Shafiq   +7 more
wiley   +1 more source

Coexistence of Localized and Systemic Juvenile Scleroderma: A Case Report and Review of Literature

open access: yesClinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Juvenile scleroderma (JS) is a rare chronic connective tissue disorder characterized by progressive fibrosis of the skin and soft tissues with/without internal organ involvements. Scleroderma manifests itself in both systemic (SSc) and localized (LS) forms.
Aye Miremarati   +4 more
wiley   +1 more source

Unveiling Parry-Romberg Syndrome With Native Demyelinating Etiology as the Underlying Cause

open access: yesActa Medica Iranica
Parry-Romberg Syndrome (PRS) is an atypical condition characterized by hemiatrophy of the face. Despite its rarity, the precise pathophysiological processes underlying its etiology remain elusive.
Kaveh Bahram   +4 more
doaj   +1 more source

Progressive hemifacial atrophy (Parry-Romberg Syndrome)

open access: yesContemporary Clinical Dentistry, 2012
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.
S A Deshingkar   +3 more
doaj   +1 more source

Sclerosing diseases of the skin

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 10, Page 1282-1301, October 2025.
Summary Sclerosing skin diseases comprise a group of distinct dermatological conditions characterized by fibrotic changes that may severely impair patients’ quality of life. These conditions often present with cutaneous manifestations and, in some cases, may extend to extracutaneous tissues, potentially resulting in significant morbidity and mortality.
Yasamin Kalantari   +4 more
wiley   +1 more source

Parry-Romberg syndrome: an unusual case of lagophthalmus and exposure keratopathy

open access: yesOral and Maxillofacial Surgery Cases, 2015
Parry-Romberg syndrome (PRS) is a poorly understood degenerative disease characterized by atrophy affecting one side of the face. In this report, we describe a patient with PRS associated with exposure keratopathy and corneal ulceration as a result of ...
Pouya M. Vakilian, BS   +2 more
doaj   +1 more source

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

Parry-Romberg Syndrome: a Rare Case Report

open access: yeseJournal of Oral Maxillofacial Research, 2011
Background: The purpose of this report is to present a rare entity of Parry-Romberg syndrome. This poorly understood degenerative condition is characterised by atrophic changes affecting one side of the face.
Anusha Laxman Rangare   +3 more
doaj  

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

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