Results 81 to 90 of about 276,835 (194)

ePoster

European Journal of Neurology, Volume 33, Issue S1, June 2026.
wiley   +1 more source

Cerebral hemiatrophy (Dyke-Davidoff-Masson syndrome) in childhood: Clinicoradiological analysis of 19 cases

, 2007
Background: The purpose of this study was to emphasize the clinical and imaging findings of 19 child cases of cerebral hemiatrophy. Methods:A total of 11 male and eight female patients underwent assessment with computed tomography and magnetic resonance ...
Atalar, Mehmet H., Tas, Fikret, Icagasioglu, Dilara   +2 more
core   +1 more source

The Phakomatosis (Neurocutaneous Syndromes): Sturge-Weber Syndrome

مجله دانشکده پزشکی اصفهان, 2008
Neurocutaneous syndromes or phakomatosis are inherited or sporadic conditions that feature lesions of both skin and nervous system. Sturge-weber syndrome (SWS) is characterized by a facial cutaneaous angioma (port-wine nevus) and an associated ...
Ahmad Chitsaz
doaj  

Dyke-Davidoff-Masson Syndrome Following Head Trauma: Clinical and Radiologic Findings

Archives of Epilepsy
Dyke-Davidoff-Masson syndrome (DDM) is an unusual condition characterized by facial asymmetry, hemiparesis, mental retardation, learning disabilities, sensorineural hearing loss, psychiatric disorders, and epilepsy.
Muhittin Emre Altunrende, Elif Evrim Ekin   +1 more
doaj   +1 more source

Marked hemiatrophy in carriers of Duchenne muscular dystrophy

, 2010
OBJECTIVE: To describe the clinical and molecular genetic findings in 2 carriers of Duchenne muscular dystrophy (DMD) who exhibited marked hemiatrophy. Duchenne muscular dystrophy is an X-linked disorder in which affected male patients harbor mutations ...
Holton, Janice L., Yau, Shu C., Yousry, Tarek, Dunand, Murielle, Farmer, Simon, Abbs, Stephen, Thonney, Francine, Rajakulendran, Sanjeev, McCauley, Joanna, Hanna, Michael G., Kuntzer, Thierry, Storey, Helen, Lobrinus, Johannes Alexander, Ashton, Emma J., Leturcq, France, Shu C. Yau, Murielle Dunand, France Leturcq, Michael G. Hanna, Tarek Yousry, Janice L. Holton, Helen Storey, Francine Thonney, Sanjeev Rajakulendran, Simon Farmer, Thierry Kuntzer, Johannes A. Lobrinus, Joanna McCauley, Stephen Abbs, Emma J. Ashton   +29 more
core   +2 more sources

A case of Dyke-Davidoff-Masson syndrome

, 2012
Dyke-Davidoff-Masson syndrome is a condition characterized by seizures, facial asymmetry, contralateral hemiplegia or hemiparesis and mental retardation. The clinical findings may be of variable degree according to the extent of brain injury.
Ali Yikilmaz, GÜMÜŞ, HAKAN, Yikilmaz, Ali, Soylu, Pembe, Poyrazoglu, Hatice Gamze, Hakan Gumus, Huseyin Per, Hatice Poyrazoglu, Mehmet Canpolat, Kumandas, Sefer, PER, HÜSEYİN, CANPOLAT, MEHMET, Pembe Soylu, Sefer Kumandas   +13 more
core   +1 more source

Late-onset Parry-Romberg Syndrome with atypical neurological manifestations: A case report

Radiology Case Reports
Parry-Romberg Syndrome (PRS) is a rare neurocutaneous disorder characterized by gradual facial hemiatrophy. We present a case study of a 64-year-old woman with late-onset PRS and linear scleroderma.
Sema Akkus, MD, Suban Amatya, MD, Kriti Shrestha, MD, Shitiz Sriwastava, MD, Demetrios A. Karides, MD   +4 more
doaj   +1 more source

Dyke-Davidoff-Masson Syndrome- a rare cause of refractory epilepsy.

Iranian Journal of Psychiatry, 2014
Dyke-Davidoff-Masson Syndrome (DDMS) is a syndrome associated with refractory epilepsy. DDMS is a rare syndrome characterized by seizures, facial asymmetry, contralateral hemiplegia and mental retardation.
Prerna Malik, Rajinder Garg, Anil Kumar D Gulia, Joginder Kario   +3 more
doaj  

Síndrome de Romberg: uma série de casos

Revista Brasileira de Cirurgia Plástica
INTRODUÇÃO: A síndrome de Romberg é uma moléstia descrita há mais de um século e, nesse período, recebeu várias denominações. É caracterizada por lenta e progressiva atrofia dos tecidos de uma hemiface, podendo acometer todos os tecidos e apresentar ...
Isis Juliane Guarezi Nasser, Priscilla Balbinot, Adriana Sayuri Kurogi Ascenço, Ivan Maluf Junior, Dirlene Taysa Berri, Marlon Câmara Lopes, Patrícia Bigolin, Willian Itikawa, Renato da Silva Freitas   +8 more
doaj   +1 more source

Síndrome de Parry-Romberg: hemiatrofia facial progresiva. Reporte de Caso.: Síndrome de Parry-Romberg.

, 2020
Introduction: Parry-Romberg Syndrome is a neurocutaneous disorder, very rare and characterized by progressive facial hemiatrophy, the first clinical sign is facial asymmetry. SPR occurs simultaneously with high frequency with linear scleroderma.
Mejía Escobar, Cinthya Karina, Sánchez Sierra, Luis Enrique, Salgado, Ana Luisa   +2 more
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