Results 11 to 20 of about 587 (146)

Cell-Assisted Lipotransfer for the Treatment of Parry-Romberg Syndrome [PDF]

open access: yesArchives of Plastic Surgery, 2012
Progressive facial hemiatrophy, also known as Parry-Romberg syndrome, is a progressive and self-limited deformation of the subcutaneous tissue volume on one side of the face that creates craniofacial asymmetry.
Yanko Castro-Govea   +6 more
doaj   +2 more sources

Progressive facial hemiatrophy (a case report)

open access: yesIndian Journal of Ophthalmology, 1973
Parmar I.P.S   +3 more
doaj   +2 more sources

PARRY ROMBERG SYNDROME [PDF]

open access: yesRomanian Journal of Rheumatology, 2016
Parry-Romberg syndrome, which is also known as progressive facial hemiatrophy, is a variant of localized scleroderma. This is a rare condition (OMIM # 141300), characterized by a progressive but self-limited atrophy of the skin and subcutaneous tissue on
Alexis-Virgil Cochino   +2 more
doaj   +1 more source

Karl Grassmann's 1896 paper “critical overview of contemporary theories of the heredity of the psychoses”

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Volume 192, Issue 3-4, Page 41-52, April-June 2023., 2023
Abstract Four years before the rediscovery of Mendel's work in 1900, Karl Grassmann published a detailed, scholarly review of the heredity of psychosis which we here review. A full translation is in the appendix. We emphasize seven major conclusions from this review.
Kenneth S. Kendler, Astrid Klee
wiley   +1 more source

Progressive hemifacial atrophy Parry Romberg syndrome characteristics of craniofacial morphology [PDF]

open access: yesStomatološki glasnik Srbije, 2007
The aim of this case report was to analyze clinical finding in a patient with rare, Parry Romberg syndrome. The patient was diagnosed with progressive facial hemiatrophy that affected skin, subcutaneous tissue and underlying bony structures.
Nikodijević-Latinović Angelina
doaj   +1 more source

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

Epilepsy and inborn errors of metabolism in adults: The diagnostic odyssey of a young woman with medium‐chain acyl‐coenzyme A dehydrogenase deficiency

open access: yesEpilepsia Open, Volume 7, Issue 4, Page 810-816, December 2022., 2022
Abstract We describe a case of epileptic encephalopathy in a young woman with undiagnosed medium‐chain acyl‐coenzyme A dehydrogenase deficiency (MCADD), who presented with an early‐onset focal motor status epilepticus (SE) then followed by permanent left hemiplegia and drug‐resistant epilepsy with neurodevelopmental delay.
Ilaria Cani   +13 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

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