Results 81 to 90 of about 1,771 (170)

Anesthetic Considerations of Patient with Parry Romberg Syndrome

open access: yesCase Reports in Clinical Practice, 2018
Parry Romberg syndrome is a rare progressive degenerative disease characterized by unilateral atrophy affecting the skin, connective tissue, muscle, and bone, typically occurs in children and young adults.
Sussan Soltani Mohammadi   +2 more
doaj  

How I explore ... eyebrow alopecia [PDF]

open access: yes, 2009
peer reviewedThe rarefaction or loss of eyebrow hair may represent an esthetic complaint or a peculiar finding associated with a given disease. The causal disorders correspond to a few dermatitides and several endocrine, auto-immune, infectious ...
Devillers, Céline   +2 more
core  

Waardenburg syndrome: A rare case

open access: yesOman Journal of Ophthalmology, 2018
Waardenburg Syndrome is a rare disorder of neural crest cell development. It is genetically inherited. Varying in prevalence from 1:42000 to 1:50,000, it compromises approximately 2-5% of congenital deaf children.
Shivlal M Rawlani   +3 more
doaj   +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

Preoperative planning for advanced modelling of anterolateral thigh flaps in the treatment of severe haemifacial atrophy in Parry–Romberg and Goldenhar syndrome

open access: yesJPRAS Open, 2018
Background: Technological advancement in medical science is constantly innovating solutions to the varied and complex challenges of surgery. Digital diagnostics and prospective microsurgery are rapidly evolving.
Kamil Firudinovich Abdullaev   +5 more
doaj   +1 more source

An overlap case of Parry–Romberg syndrome and en coup de sabre with striking ocular involvement and anti-double-stranded DNA positivity

open access: yesIndian Journal of Ophthalmology, 2018
Parry–Romberg syndrome (PRS) may overlap localized scleroderma (morphea) lesions with linear depression (en coup de sabre [ECDS]). Overlap case with PRS and ECDS was presented.
Hatice Atas   +4 more
doaj   +1 more source

Case of Rapid Progression of Hemiatrophy on the Face: A New Clinical Entity?

open access: yesCase Reports in Dermatological Medicine, 2015
A lot of diseases, including lupus profundus, morphea, lipodystrophy, and Parry-Romberg syndrome, may manifest progressive hemifacial atrophy. These diseases usually progress slowly and rapid progression of atrophy is extremely rare.
Hisashi Nomura   +3 more
doaj   +1 more source

Progressive hemifacial atrophy

open access: yesDental Research Journal, 2013
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 but self-limited atrophy affecting one side of the face.
Abhijeet Sande   +3 more
doaj   +1 more source

Idiopathic acquired progressive left facial hemiatrophy (Parry-Romberg syndrome) in a 21-year-old man in semi-urban, south-west Nigeria [PDF]

open access: yes, 2011
Idiopathic progressive hemifacial atrophy, or Parry-Romberg syndrome, is a rare entity, seldom described in medical texts. Though first described in 1825, as yet there are no clear-cut diagnostic criteria. It is of interest mainly because of the numerous
Imarhiagbe, FA
core   +1 more source

Pathogenesis, diagnosis and treatment of Rasmussen encephalitis: A European consensus statement [PDF]

open access: yes, 2017
Rasmussen encephalitis (RE) is a rare but severe immune-mediated brain disorder leading to unilateral hemispheric atrophy, associated progressive neurological dysfunction and intractable seizures.
Antozzi, C.   +10 more
core  

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