Results 21 to 30 of about 587 (146)
An unusual case of Dyke–Davidoff–Masson syndrome revealed by status epilepticus in a Malian patient
Clinical Case Reports, Volume 10, Issue 10, October 2022., 2022 Abstract The Duke–Davidoff–Masson syndrome (DDMS) is a rare neurological condition with unknown prevalence, globally. To date, <100 cases have been reported worldwide. We report the case of an 18‐year‐old patient admitted for status epilepticus seizure, and who presented a right hemiparesis, body asymmetry, joints ankylosis, and mental retardation ...
Samba O. Djimdé +8 more
wiley +1 more source
Parry-Romberg Syndrome: A Case of Late Onset with Rapid Progression [PDF]
Journal of Clinical and Diagnostic Research, 2014 Parry–Romberg syndrome (PRS) or progressive hemifacial atrophy is rare, poorly understood condition with an unclear aetiology and characterized by slow and progressive atrophy affecting one side of the face.
Senthil Kumar +4 more
doaj +1 more source
Epilepsia, Volume 63, Issue 6, Page 1443-1474, June 2022., 2022 Abstract The goal of this paper is to provide updated diagnostic criteria for the epilepsy syndromes that have a variable age of onset, based on expert consensus of the International League Against Epilepsy Nosology and Definitions Taskforce (2017–2021).
Kate Riney +19 more
wiley +1 more source
Parry Romberg syndrome: A rare case report
Journal of Indian Academy of Oral Medicine and Radiology, 2014 The Parry Romberg syndrome (PRS) is a rare neurocutaneous disorder characterized by progressive facial hemiatrophy. Parry Romberg syndrome is characterized by a slow progressive atrophy that appears in the early stages of life, primarily affecting the ...
Raj Kumar Badam +3 more
doaj +1 more source
Mendelian etiologies identified with whole exome sequencing in cerebral palsy
Annals of Clinical and Translational Neurology, Volume 9, Issue 2, Page 193-205, February 2022., 2022 Abstract Objectives Cerebral palsy (CP) is the most common childhood motor disability, yet its link to single‐gene disorders is under‐characterized. To explore the genetic landscape of CP, we conducted whole exome sequencing (WES) in a cohort of patients with CP.
Maya Chopra +38 more
wiley +1 more source
Parry-Romberg Syndrome Associated with Localized Scleroderma
Case Reports in Neurology, 2010 Parry-Romberg syndrome is a rare neurocutaneous disorder of unknown origin. It is characterized by progressive facial hemiatrophy and frequently overlaps with a condition known as linear scleroderma ‘en coup de sabre’.
Jelena Maletic +4 more
doaj +1 more source
Idiopathic hemifacial atrophy successfully treated with hyaluronic acid filler: About two new cases
, 2023 Journal of Cosmetic Dermatology, Volume 22, Issue 3, Page 1142-1145, March 2023.
Kouki Chaima +2 more
wiley +1 more source
Adult Presentation of Dyke-Davidoff-Masson Syndrome: A Case Report
Case Reports in Neurology, 2016 Dyke-Davidoff-Masson syndrome (DDMS) is a rare disease which is clinically characterized by hemiparesis, seizures, facial asymmetry, and mental retardation.
Ujjawal Roy +3 more
doaj +1 more source
Parry-Romberg syndrome with ipsilateral hemipons involvement presenting as monoplegic ataxia [PDF]
Korean Journal of Pediatrics, 2015 Parry-Romberg syndrome (PRS) is a rare, acquired disorder characterized by progressive unilateral facial atrophy of the skin, soft tissue, muscles, and underlying bony structures that may be preceded by cutaneous induration.
Yun-Jin Lee +4 more
doaj +1 more source
Oral manifestations of Parry-Romberg syndrome: A review of literature
Avicenna 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