Results 21 to 30 of about 832 (143)

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

Exacerbation of secondary trigeminal neuralgia due to osteomyelitis in a case of Romberg facial hemiatrophy [PDF]

open access: yesRomanian Journal of Neurology, 2011
Progressive facial hemiatrophy or Romberg syndrome, is a sporadic disease of unknown etiology characterized by progressive and self limited shrinking and deformation of one hemiface accompanied by various neurologic complication, including trigeminal ...
Florin Popovici   +3 more
doaj   +1 more source

A case report of Parry Romberg Syndrome initially presenting as periodontitis [PDF]

open access: yes, 2018
Parry Romberg Syndrome (PRS) is a rare disorder of progressive hemifacial atrophy, involving soft tissues, fat and occasionally bone. It can co-exist with presentations of Morphea.
Bramley   +14 more
core   +1 more source

An unusual case of Dyke–Davidoff–Masson syndrome revealed by status epilepticus in a Malian patient

open access: yesClinical 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

Progressive facial hemiatrophy (Parry-Romberg syndrome): short case report

open access: yesJournal of Oral Medicine and Oral Surgery, 2019
Introduction: The Parry Romberg syndrome (PRS) is a mosaic disease of unknown aetiology which mostly affects women. The facial hemiatrophy generally begins during the early childhood.
Puidupin Alexandre   +4 more
doaj   +1 more source

Parry-Romberg Syndrome: A Case of Late Onset with Rapid Progression [PDF]

open access: yesJournal 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

Parry-Romberg syndrome: A case with a possible association with lyme disease [PDF]

open access: yes, 2015
Parry-Romberg syndrome is an acquired slowly progressive disease characterized by an atrophy mostly involving half of the face. The pathogenesis of this disfiguring condition is still controversial.
Di Meo, N.   +4 more
core   +2 more sources

International League Against Epilepsy classification and definition of epilepsy syndromes with onset at a variable age: position statement by the ILAE Task Force on Nosology and Definitions

open access: yesEpilepsia, 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

Clinical evaluation of techniques used in the surgical treatment of progressive hemifacial atrophy [PDF]

open access: yes, 1994
We critically review 13 patients with progressive hemifacial atrophy treated with three basic surgical procedures (free flap transplantation, alloplastic implants, micro-fat injections ‘lipofilling’) and further ancillary techniques.
Gilbert, P.M. (Philip)   +5 more
core   +2 more sources

Mendelian etiologies identified with whole exome sequencing in cerebral palsy

open access: yesAnnals 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

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