A case of parasympathetic hyperactivity and associated Parry–Romberg syndrome
SAGE Open Medical Case Reports, 2021 This case report describes a 46-year-old female with a history of multiple endocrine neoplasia type 1 syndrome status post-parathyroidectomy, thymectomy via robotic video-assisted thoracoscopic surgery, and pituitary adenoma resection presenting with ...
Andrea N Clapp, Anna DePold Hohler
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Dyke‐Davidoff‐Masson syndrome—A rare cause of recurrent seizures in adulthood
Clinical Case Reports, Volume 12, Issue 6, June 2024.Key Clinical Message It is important to consider DDMS as a differential diagnosis in any patient with early childhood onset of epilepsy. Early diagnosis and optimal management are key to reducing the disabling effect of DDMS.
Patricia Afrim +6 more
wiley +1 more source
Przegląd Dermatologiczny, 2011 Introduction. Progressive facial hemiatrophy (Parry-Romberg syndrome)is a relatively rare disease of unclear aetiology. Some authorspostulate its relation with linear scleroderma.Objective.
Ligia Brzezińska-Wcisło +2 more
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MR and CT imaging in the Dyke-Davidoff-Masson syndrome: report of three cases and contribution to pathogenesis and differential diagnosis [PDF]
Arquivos de Neuro-Psiquiatria, 1998 Cerebral hemiatrophy or Dyke-Davidoff-Masson syndrome is a condition characterized by seizures, facial asymmetry, contralateral hemiplegia or hemiparesis, and mental retardation.
PAULO HENRIQUE AGUIAR +7 more
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S2k guideline: Diagnosis and therapy of localized scleroderma
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 4, Page 605-620, April 2024.Summary The updated S2k guideline deals with the diagnosis and therapy of localized scleroderma (LoS). LoS represents a spectrum of sclerotic skin diseases in which, depending on the subtype and localisation, structures such as adipose tissue, muscles, joints, and bones may also be affected.
Alexander Kreuter +12 more
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Oral manifestations of Parry-Romberg syndrome: A review of literature
Avicenna Journal of Medicine, 2015 Parry-Romberg syndrome (PRS) or progressive facial hemiatrophy is a developmental craniofacial disorder of unknown etiology characterized by a slowly progressive unilateral facial atrophy.
Nader A Al-Aizari +4 more
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Exacerbation of secondary trigeminal neuralgia due to osteomyelitis in a case of Romberg facial hemiatrophy [PDF]
Romanian 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
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Zespolenie nerwu twarzowego z połową nerwu podjęzykowego w leczeniu porażenia nerwu twarzowego [PDF]
, 1970 Background and purpose Commonly used classic hypoglossal (CN XII) to facial nerve (CN VII) anastomosis has the disadvantage of tongue hemiatrophy. Thus, various attempts have been made to modify this method to reduce the tongue damage.
Bartoszewicz, Robert +3 more
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Rasmussen’s Encephalitis [PDF]
, 2022 Introduction: Rasmussen’s encephalitis (RE) is an inflammatory encephalopathy characterized by progressive refractory focal seizures, cognitive deterioration and focal neurological deficit that occur with gradual atrophy of one brain hemisphere ...
Gaurav Dave +6 more
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Pyogenic Granuloma in a Patient of Sturge-Weber Syndrome with Bilateral Port Wine Stain- A Rare Case Report [PDF]
, 2014 Sturge-Weber syndrome (SWS) also known as encephalotrigeminal angiomatosis. It is a neurocutaneous syndrome, characterized by a facial vascular birthmark and neurological abnormalities.
Mamata G. P +3 more
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