Results 21 to 30 of about 755 (130)

A Complex Inflammatory Triad: A Rare Case of Parry‐Romberg Syndrome With Systemic Lupus Erythematosus and Thyroiditis

Clinical Case Reports, Volume 14, Issue 4, April 2026.
ABSTRACT Parry‐Romberg Syndrome (PRS) is a rare disorder characterized by progressive unilateral facial atrophy, traditionally viewed as a localized scleroderma variant. Its rare coexistence with systemic lupus erythematosus (SLE) and autoimmune thyroiditis (AIT) suggests a broader inflammatory etiology, challenging the notion of PRS as a purely ...
Sakib Abrar, Fabiha Rahman Spriha, Sajjad Ghanim Al‐Badri, Md. Imran Hossain, Ibrahim Khalil   +4 more
wiley   +1 more source

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

Clinical 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, Hafiza Manahil Majeed, Hamza Hafeez Farooqi, Muhammad Waqar Khaliq, Danish Ali Chohan, Awais Mushtaq, Ali Gohar, Muhammad Husnain Ahmad   +7 more
wiley   +1 more source

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

Clinical 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, Kosar Babaeian Roshani, Manijeh Tabrizi, Fatemeh Tahghighi Sharabian, Seyyedeh Azade Hoseini Nouri   +4 more
wiley   +1 more source

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

Acta 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, Mohammad Ali Nahayati, Mohammad Shariati, Ayoub Tavakolian, Hussein Sharare   +4 more
doaj   +1 more source

Progressive hemifacial atrophy (Parry-Romberg Syndrome)

Contemporary 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, S R Barpande, J D Bhavthankar, J G Humbe   +3 more
doaj   +1 more source

Sclerosing diseases of the skin

JDDG: 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, Katharina Meier, Kamran Ghoreschi, Maria Kinberger, Farzan Solimani   +4 more
wiley   +1 more source

Sklerosierende Erkrankungen der Haut

JDDG: 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, Katharina Meier, Kamran Ghoreschi, Maria Kinberger, Farzan Solimani   +4 more
wiley   +1 more source

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   +1 more source

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

Oral 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, Richard M. Kline, MD, Zachary S. Peacock, DMD, MD   +2 more
doaj   +1 more source

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

The 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, Allen Green, Jon‐Paul Pepper, Sarah R. Akkina   +3 more
wiley   +1 more source