Results 71 to 80 of about 1,837 (197)
Peripheral nervous system involvment in localized scleroderma with facial hemiatrophy [PDF]
, 1991 woman with facial hemiatrophy and ...
Tola M. R. +4 more
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Dyke-Davidoff-Masson Syndrome as a rare congenital hemiatrophy: a case report: Dyke-Davidoff-Masson Syndrome [PDF]
, 2021 Introduction: Dyke-Davidoff-Masson syndrome (DDMS) is a rare condition in childhood with very few cases reported in sub-Saharan Africa. Typically, the patient presents with facial asymmetry, seizures, and hemiparesis.
Nwako, Azubuike Benjamin +3 more
core +1 more source
A review of pediatric cerebral hemiatrophy: a series of cases
MGM Journal of Medical SciencesCerebral hemiatrophy represents a spectrum of neurological disorders marked by unilateral cerebral atrophy, often resulting in significant neurological and functional impairments.
Sumedha Varshney +5 more
doaj +1 more source
Adult Presentation of Dyke-Davidoff-Masson Syndrome: A Case Report
Case Reports in Neurology, 2016 Dyke-Davidoff-Masson syndrome (DDMS) is a rare disease which is clinically characterized by hemiparesis, seizures, facial asymmetry, and mental retardation.
Ujjawal Roy +3 more
doaj +1 more source
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
Psychoses of Epilepsy: Unravelling the Phenotypic and Genotypic Features
Annals of Neurology, Volume 98, Issue 1, Page 35-47, July 2025.Objectives We analyzed the genotypic and phenotypic features of patients with psychosis of epilepsy (POE). Methods Patients with POE recruited to an epilepsy genetics research program underwent phenotyping and genetic analysis. The latter included screening for rare pathogenic variants in epilepsy genes, and polygenic risk score (PRS) calculation for ...
Genevieve Rayner +4 more
wiley +1 more source
Arquivos de Neuro-Psiquiatria, 2004 Unilateral destructive brain lesions of early development can result in compensatory thickening of the ipsilateral cranial vault. The aim of this study was to determine the frequency of these bone changes among patients with epilepsy and precocious ...
Teixeira Ricardo A. +7 more
doaj
Progressive facial hemiatrophy with associated osseous lesions [PDF]
, 2007 Progressive facial hemiatrophy (PFH) is a rare condition characterized by the slow, progressive appearance of a unilateral facial atrophy that affects the skin, subcutaneous tissue, muscle and bone.
Pérez Oliva, Narciso +4 more
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Hemiatrofia facial de romberg: relato de caso Romberg's facial hemiatrophy: case report [PDF]
, 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.
Johnny Wesley G. Martins +3 more
core +2 more sources
Natural History of Rasmussen’s Syndrome
Pediatric Neurology Briefs, 2002 Seizure frequency, degree of hemiparesis and cerebral hemiatrophy are analysed in 13 patients with histopathologically proven Rasmussen’s encephalitis (RE) examined at the University of Bonn, Germany.
J Gordon Millichap
doaj +1 more source