Results 61 to 70 of about 276,835 (194)

Oral manifestations of Parry-Romberg syndrome: A review of literature

open access: yesAvicenna Journal of Medicine, 2015
Parry-Romberg syndrome (PRS) or progressive facial hemiatrophy is a developmental craniofacial disorder of unknown etiology characterized by a slowly progressive unilateral facial atrophy.
Nader A Al-Aizari   +4 more
doaj   +1 more source

A case of parasympathetic hyperactivity and associated Parry–Romberg syndrome

open access: yesSAGE 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   +1 more source

Dyke‐Davidoff‐Masson syndrome—A rare cause of recurrent seizures in adulthood

open access: yesClinical Case Reports, Volume 12, Issue 6, June 2024.
Key Clinical Message It is important to consider DDMS as a differential diagnosis in any patient with early childhood onset of epilepsy. Early diagnosis and optimal management are key to reducing the disabling effect of DDMS.
Patricia Afrim   +6 more
wiley   +1 more source

Neurologic abnormalities in two patients with facial hemiatrophy and sclerosis coexisting with morphea

open access: yes, 1997
Progressive facial hemiatrophy or Parry-Romberg syndrome is a rare entity characterized by unilateral atrophy of the skin, subcutaneous tissue, and the underlying bony structures. This syndrome has many features of linear scleroderma en coup de sabre but
E. Passoni, S. Menni, A.V. Marzano
core   +1 more source

MR and CT imaging in the Dyke-Davidoff-Masson syndrome: report of three cases and contribution to pathogenesis and differential diagnosis [PDF]

open access: yesArquivos de Neuro-Psiquiatria, 1998
Cerebral hemiatrophy or Dyke-Davidoff-Masson syndrome is a condition characterized by seizures, facial asymmetry, contralateral hemiplegia or hemiparesis, and mental retardation.
PAULO HENRIQUE AGUIAR   +7 more
doaj   +1 more source

S2k guideline: Diagnosis and therapy of localized scleroderma

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 4, Page 605-620, April 2024.
Summary The updated S2k guideline deals with the diagnosis and therapy of localized scleroderma (LoS). LoS represents a spectrum of sclerotic skin diseases in which, depending on the subtype and localisation, structures such as adipose tissue, muscles, joints, and bones may also be affected.
Alexander Kreuter   +12 more
wiley   +1 more source

Cerebral Hemiatrophy: Etiology and Pathology

open access: yes, 1991
Two types of cerebral hemiatrophy are reported from the Institute of Neuropathology at the University of Giessen, Arndtstrafse ...
J Gordon Millichap
core   +1 more source

Automatic facial analysis for objective assessment of facial paralysis [PDF]

open access: yes, 2009
Facial Paralysis is a condition causing decreased movement on one side of the face. A quantitative, objective and reliable assessment system would be an invaluable tool for clinicians treating patients with this condition. This paper presents an approach
McGrenary, Stewart   +3 more
core   +2 more sources

Parry-Romberg syndrome with multiple intracranial cysts: A rare case report

open access: yesJournal of Pediatric Neurosciences, 2016
Parry-Romberg syndrome (PRS) is a rare, poorly understood degenerative condition characterized by atrophic changes affecting one side of the face. The cause of these changes remains obscure.
Rakesh Gupta, Harshad Patil
doaj   +1 more source

Overlap between linear scleroderma, progressive facial hemiatrophy and immune-inflammatory encephalitis in a paediatric cohort

open access: yes, 2015
Linear scleroderma en coup the sabre (LSCS), progressive facial hemiatrophy (PFH) and autoimmune encephalitis are distinct clinical entities, although patients with overlapping features have been reported.
Despontin, Karine   +6 more
core   +1 more source

Home - About - Disclaimer - Privacy