Results 11 to 20 of about 832 (143)
Adult Presentation of Dyke-Davidoff-Masson Syndrome, a Radiological Enigma: A Case Report. [PDF]
Case Rep RadiolIntroduction and Importance: Dyke–Davidoff–Masson syndrome (DDMS) is a rare neurological condition characterized by focal or generalized drug‐resistant epilepsy, hemiparesis, face or body asymmetry with atrophy, and cognitive impairment in early childhood and adulthood. DDMS is generally diagnosed in the paediatric age group.
Paudel S +5 more
europepmc +2 more sources
Idiopathic acquired progressive left facial hemiatrophy (Parry-Romberg syndrome) in a 21-year-old man in semi-urban, south-west Nigeria [PDF]
South African Family Practice, 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
F.A. Imarhiagbe, A.O. Adeoti
doaj +3 more sources
Hemiatrofia facial de romberg: relato de caso Romberg's facial hemiatrophy: case report [PDF]
Arquivos de Neuro-Psiquiatria, 1995 Os autores apresentam o caso de uma paciente de 45 anos de idade com história de 15 meses de evolução, de hemiatrofia progressiva da face e língua à esquerda.
Nicandro De Figueiredo Neto +3 more
doaj +2 more sources
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 +4 more sources
Romanian 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
Progressive hemifacial atrophy: a review [PDF]
, 2015 BACKGROUND: Progressive Hemifacial Atrophy (PHA) is an acquired, typically unilateral, facial distortion with unknown etiology. The true incidence of this disorder has not been reported, but it is often regarded as a subtype of localized scleroderma ...
Megha M Tollefson +2 more
core +4 more sources
American 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
Scleroderma and dentistry: Two case reports [PDF]
, 2016 © 2016 The Author(s).Background: Scleroderma is a chronic connective tissue disorder with unknown etiology. It is characterized by excessive deposition of extracellular matrix in the connective tissues causing vascular disturbances which can result in ...
Bornstein, Michael M. +4 more
core +3 more sources
Progressive hemifacial atrophy Parry Romberg syndrome characteristics of craniofacial morphology [PDF]
Stomatološki 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
Epilepsia 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