Results 61 to 70 of about 844,102 (172)
Rwanda Medical Journal, 2022 Lennox-Gastaut syndrome (LGS) is a form of severe epileptic encephalopathy in children. LGS with encephalomalacia cysts is rare in children. We report a six-year-old mentally retarded boy who was referred for an intractable seizure.
P. I. Gunawan, W. Suryaningtyas
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Dyke-Davidoff-Masson syndrome presenting with recurrent seizures [PDF]
Romanian Journal of Neurology, 2016 Dyke-Davidoff-Masson syndrome (DDMS) is cerebral hemiatrophy occurring following brain insult resulting from infarct, trauma or infection in utero or soon after birth.
M. Rajaguru +4 more
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Sclerosing diseases of the skin
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 10, Page 1282-1301, October 2025.Summary Sclerosing skin diseases comprise a group of distinct dermatological conditions characterized by fibrotic changes that may severely impair patients’ quality of life. These conditions often present with cutaneous manifestations and, in some cases, may extend to extracutaneous tissues, potentially resulting in significant morbidity and mortality.
Yasamin Kalantari +4 more
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Adult Presentation of Dyke Davidoff Masson Syndrome With Schizoaffective Disorder — A Case Report
Kerala Journal of Psychiatry, 2018 Dyke Davidoff Masson syndrome (DDMS) is a rare disease with characteristic radiological features, seizures, mental retardation, facial asymmetry, and psychiatric manifestations. Here, we report a case of a 50-year-old female who had a refractory seizure
MK Dinesh Kumar, Denver Steven Pinto
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Epidermal Nevi and Epidermal Naevus Syndromes
JEADV Clinical Practice, Volume 4, Issue 3, Page 669-680, August 2025.ABSTRACT Epidermal nevi (EN) arise from postzygotic variants in ectoderm‐derived cell lines, such as keratinocytes and cells forming adnexa. EN may be present alone without any associated abnormality or be part of a syndrome. In this review, we will discuss about the clinical and genetics of the main types of EN and related syndromes.
Gianluca Tadini +2 more
wiley +1 more source
Dyke-Davidoff-Masson syndrome in an 8-year-old child: Report of a case
Radiology Case ReportsDyke-Davidoff-Masson syndrome (DDMS) is a rare entity. Few cases have been described in the literature. It can be symptomatic or asymptomatic. The clinical signs are very varied. Imaging is the key to diagnosis.
Nourrelhouda Bahlouli +6 more
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, 2017 Childhood cerebral hemiatrophy or Dyke-Davidoff-Masson syndrome is very rare in our locality. characterized by symmetrical calcifications noticeable in parts of the brain.
Danfulani Mohammed +4 more
semanticscholar +1 more source
Progressive facial and cerebral hemiatrophy
Cleveland Clinic Journal of Medicine, 1984 A 43-year-old woman with progressive facial hemiatrophy had contralateral hemianopia and sensory loss. A computed-tomographic brain scan showed ipsilateral cerebral atrophy. The neurological and neuroradiological features of progressive facial hemiatrophy are reviewed.
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Progressive facial hemiatrophy (Parry-Romberg syndrome) with ipsilateral cerebral hemiatrophy [PDF]
Neurology, 2010 The authors report a case of Progressive facial hemiatrophy (Parry-Romberg syndrome) with ipsilateral cerebral hemiatrophy; they underline how the clinical aspect of atrophy is concordant with MRI of the brain and soft tissue that shows cerebral omolateral atrophy and lack of the ipsilateral soft facial tissue.
RESTIVO D. A, MILONE, Pietro
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Acquired Dyke-Davidoff-Masson syndrome (DDMS)
International Journal of Advanced Medical and Health Research, 2015 Dyke-Davidoff-Masson syndrome (DDMS) is characterized by cerebral hemiatrophy, contralateral hemiplegia, skull and facial asymmetries, seizures, and mental retardation. We present a case of acquired DDMS following meningoencephalitis.
Jitender Aneja +3 more
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