Results 61 to 70 of about 119,743 (184)

Demyelinating etiology as a possible cause of Parry–Romberg Syndrome (PP-14) [PDF]

open access: yesNeurology Letters, 2023
Parry–Romberg syndrome (PRS) is a rare disease that causes hemiatrophy of the face. The pathophysiological mechanisms involved in its etiology are unknown, but several previous reports suggest the involvement of autoimmune factors.
K. Bahrami   +2 more
doaj  

Surgical Management of Progressive Hemifacial Atrophy With De-Epithelialized Profunda Artery Perforator Flap [PDF]

open access: yes, 2017
Progressive hemifacial atrophy (PHA) is a rare disorder characterized by slow, unilateral atrophy of the soft tissues and bones of the craniofacial region. The defect becomes more pronounced with age, leading to esthetic and functional deficits. However,
Janovszky Ágnes   +3 more
core   +1 more source

Seizures and electroencephalographic findings in inborn errors of metabolism: Clues to differential diagnosis in the neonatal period, infancy, childhood and adolescence, and review of the literature

open access: yesEpileptic Disorders, Volume 27, Issue 5, Page 745-802, October 2025.
Abstract Although inborn errors of metabolism (IEM) are a rare cause of epilepsy, seizures are a common presentation in these disorders. Seizures in IEM are frequently refractory to conventional anti‐seizure medication and might warrant initiation of specific treatments based on vitamins or dietary modifications or provision of alternative substrates ...
D. Kapoor   +7 more
wiley   +1 more source

Use of intraorbital Polietigel® in a patient with progressive hemifacial atrophy: case report [PDF]

open access: yes, 2004
O objetivo é relatar o caso de portadora de atrofia hemifacial progressiva, atendida na Faculdade de Medicina de Botucatu-UNESP: A paciente do sexo feminino, 43 anos, branca, queixava-se de afundamento progressivo do olho esquerdo e região orbitária há ...
Rossa, Romualdo   +10 more
core   +2 more sources

Computer Vision Technologies in Movement Disorders: A Systematic Review

open access: yesMovement Disorders Clinical Practice, Volume 12, Issue 9, Page 1229-1243, September 2025.
Abstract Background Evaluation of movement disorders primarily relies on phenomenology. Despite refinements in diagnostic criteria, the accuracy remains suboptimal. Such a gap may be bridged by machine learning and video technology, which permit objective, quantitative, non‐invasive motor analysis.
Pasquale Maria Pecoraro   +4 more
wiley   +1 more source

The role of serial autologous fat grafting in the functional and aesthetic rehabilitation of hemifacial atrophy: a case report

open access: yesJournal of Cosmetic Medicine
Hemifacial atrophy, including Parry-Romberg syndrome, is a rare, progressive disorder characterized by unilateral loss of facial soft tissue, with or without neurologic and/or ocular manifestations.
Al Farabi Lee Jaafar   +2 more
doaj   +1 more source

Parry–Romberg Syndrome with Uhthoff’s Phenomena: A Spectrum of Autoimmune Disease?

open access: yesCase Reports in Immunology, 2019
Parry–Romberg syndrome (PRS) is a rare disorder characterized by unilateral facial atrophy. Currently, the pathogenesis of PRS is poorly understood and no definitive treatment is available.
Samuel Asanad
doaj   +1 more source

Hemifacial Spasm and Blepharospasm: Divergent Social Cognition Performance Despite Similar Neurocognitive Profiles

open access: yesBrain and Behavior, Volume 15, Issue 8, August 2025.
ABSTRACT Background Hemifacial spasm (HFS) and blepharospasm (BSP) are two neurological disorders characterized by involuntary contractions in the eye and face area. These two diagnostic groups' neurocognitive and social cognition performances are not adequately understood regarding behavioral neurology.
Samet Çelik
wiley   +1 more source

Botulinum Neurotoxins: History, Mechanism, and Applications. A Narrative Review

open access: yesJournal of Neurochemistry, Volume 169, Issue 8, August 2025.
Botulinum neurotoxins (BoNTs), produced by Clostridium botulinum, bind irreversibly to presynaptic cholinergic nerve terminals and exploit a zinc‐dependent mechanism to cleave SNARE proteins, blocking acetylcholine release and causing flaccid paralysis.
Arik Monash   +3 more
wiley   +1 more source

Parry-romberg syndrome: about a case

open access: yesThe 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

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