Results 21 to 30 of about 920 (168)
Skin Research and Technology, Volume 29, Issue 4, April 2023., 2023 Abstract Background Phacomatosis pigmentokeratotica (PPK) is a distinct and rare type of epidermal nevus syndrome characterized by coexisting nonepidermolytic organoid sebaceous nevus (SN) with one or more speckled lentiginous nevi (SLN). Atypical nevi including compound Spitz and compound dysplastic may manifest within regions of SLN.
Jenna Lee +6 more
wiley +1 more source
Progressive facial hemiatrophy (Parry-Romberg syndrome): short case report
Journal 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
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
Dyke-Davidoff-Masson syndrome: A rare case report
Medical Journal of Dr. D.Y. Patil University, 2016 Dyke-Davidoff-Masson syndrome (DDMS) is a rare clinical condition characterized by seizures, facial asymmetry, contralateral spastic hemiplegia or hemiparesis, with learning difficulties. It is also called as cerebral hemiatrophy.
Charan Singh Jilowa +3 more
doaj +1 more source
Parry Romberg syndrome: A rare case report
Journal of Indian Academy of Oral Medicine and Radiology, 2014 The Parry Romberg syndrome (PRS) is a rare neurocutaneous disorder characterized by progressive facial hemiatrophy. Parry Romberg syndrome is characterized by a slow progressive atrophy that appears in the early stages of life, primarily affecting the ...
Raj Kumar Badam +3 more
doaj +1 more source
Dyke–Davidoff–Masson syndrome with crossed cerebellar atrophy
South African Journal of Radiology, 2017 Dyke–Davidoff–Masson syndrome is a rare condition with classical, clinical and radiological changes – mental retardation, hemiparesis, facial asymmetry, seizures and cerebral hemiatrophy with calvarial changes.
Sanjay M. Khaladkar +4 more
doaj +1 more source
Dyke Davidoff Masson Syndrome with Abdominal Epilepsy-Rare Presentation
Asian Journal of Medical Sciences, 2013 Dyke Davidoff Masson Syndrome (DDMS) with abdominal epilepsy, is a rare clinical condition. It is characterized by severe abdominal pain with seizures, facial asymmetry, contralateral hemiparesis, and mental retardation.
Shitanshu Srivastava
doaj +1 more source